MiMeDB: Showing metabocard for Isoamyl phenylacetate (MMDBc0047711)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-19 15:39:08 UTC

Update Date

2022-09-01 01:47:48 UTC

Metabolite ID

MMDBc0047711

Metabolite Identification

Common Name

Isoamyl phenylacetate

Description

Isoamyl phenylacetate, or 3-methylbutyl phenylacetate is found in peppermint. 3-Methylbutyl phenylacetate is a flavouring ingredient. 3-Methylbutyl phenylacetate belongs to the family of Phenylacetic Acid Derivatives. These are compounds containing a phenylacetic acid moiety, which consists of a phenyl group substituted at the second position by an acetic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0035008
     RDKit          3D
3-Methylbutyl phenylacetate
 33 33  0  0  0  0  0  0  0  0999 V2000
    4.2375    1.4850   -0.1670 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2044    0.0090    0.0648 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2668   -0.7827   -1.2242 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9497   -0.3433    0.8289 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7008    0.0626    0.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5895   -0.3075    0.8439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7213   -0.0865    0.4428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8923    0.4600   -0.6633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7972   -0.5137    1.3523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1439   -0.2515    0.8684 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7760   -1.2189    0.1146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0634   -1.0264   -0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7180    0.1379   -0.1105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0903    1.1133    0.6452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8148    0.9251    1.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8970    1.9784    0.7869 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2567    1.8239   -0.4521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5077    1.7578   -0.9550 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0608   -0.2768    0.6995 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9231   -0.1734   -2.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6582   -1.6881   -1.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3026   -1.0667   -1.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9911    0.2042    1.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9661   -1.4199    1.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7620    1.1674   -0.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6831   -0.3802   -0.9506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6749   -1.6105    1.5145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6731   -0.0541    2.3648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3174   -2.1705   -0.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5413   -1.8070   -0.9698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7137    0.3125   -0.4775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6418    2.0182    0.8323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3774    1.7227    1.7162 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  9 27  1  0
  9 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  0
 15 33  1  0
M  END


  Mrv0541 05061308112D          

 15 15  0  0  0  0            999 V2000
    5.7158    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  2  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  2  0  0  0  0
  9  8  1  0  0  0  0
 11  1  1  0  0  0  0
 11  2  1  0  0  0  0
 11  8  1  0  0  0  0
 12  6  2  0  0  0  0
 12  7  1  0  0  0  0
 12 10  1  0  0  0  0
 13 10  1  0  0  0  0
 14 13  2  0  0  0  0
 15  9  1  0  0  0  0
 15 13  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0047711

> <DATABASE_NAME>
MIME

> <SMILES>
CC(C)CCOC(=O)CC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C13H18O2/c1-11(2)8-9-15-13(14)10-12-6-4-3-5-7-12/h3-7,11H,8-10H2,1-2H3

> <INCHI_KEY>
QWBQBUWZZBUFHN-UHFFFAOYSA-N

> <FORMULA>
C13H18O2

> <MOLECULAR_WEIGHT>
206.2808

> <EXACT_MASS>
206.13067982

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
24.049154462138546

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-methylbutyl 2-phenylacetate

> <ALOGPS_LOGP>
3.83

> <JCHEM_LOGP>
3.3678062723333326

> <ALOGPS_LOGS>
-4.03

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.086224593758343

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
60.55690000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.94e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-methylbutyl 2-phenylacetate

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0035008
     RDKit          3D
3-Methylbutyl phenylacetate
 33 33  0  0  0  0  0  0  0  0999 V2000
    4.2375    1.4850   -0.1670 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2044    0.0090    0.0648 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2668   -0.7827   -1.2242 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9497   -0.3433    0.8289 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7008    0.0626    0.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5895   -0.3075    0.8439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7213   -0.0865    0.4428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8923    0.4600   -0.6633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7972   -0.5137    1.3523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1439   -0.2515    0.8684 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7760   -1.2189    0.1146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0634   -1.0264   -0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7180    0.1379   -0.1105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0903    1.1133    0.6452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8148    0.9251    1.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8970    1.9784    0.7869 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2567    1.8239   -0.4521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5077    1.7578   -0.9550 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0608   -0.2768    0.6995 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9231   -0.1734   -2.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6582   -1.6881   -1.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3026   -1.0667   -1.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9911    0.2042    1.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9661   -1.4199    1.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7620    1.1674   -0.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6831   -0.3802   -0.9506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6749   -1.6105    1.5145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6731   -0.0541    2.3648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3174   -2.1705   -0.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5413   -1.8070   -0.9698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7137    0.3125   -0.4775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6418    2.0182    0.8323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3774    1.7227    1.7162 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  9 27  1  0
  9 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  0
 15 33  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      10.669   3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.336   5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334   5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002   3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667   3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.001   5.390   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       5.335   3.080   0.000  0.00  0.00           O+0
CONECT    1   11                                                            
CONECT    2   11                                                            
CONECT    3    4    5                                                       
CONECT    4    3    6                                                       
CONECT    5    3    7                                                       
CONECT    6    4   12                                                       
CONECT    7    5   12                                                       
CONECT    8    9   11                                                       
CONECT    9    8   15                                                       
CONECT   10   12   13                                                       
CONECT   11    1    2    8                                                  
CONECT   12    6    7   10                                                  
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15    9   13                                                       
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

COMPND    HMDB0035008
HETATM    1  C1  UNL     1       4.238   1.485  -0.167  1.00  0.00           C  
HETATM    2  C2  UNL     1       4.204   0.009   0.065  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.267  -0.783  -1.224  1.00  0.00           C  
HETATM    4  C4  UNL     1       2.950  -0.343   0.829  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.701   0.063   0.049  1.00  0.00           C  
HETATM    6  O1  UNL     1       0.589  -0.308   0.844  1.00  0.00           O  
HETATM    7  C6  UNL     1      -0.721  -0.087   0.443  1.00  0.00           C  
HETATM    8  O2  UNL     1      -0.892   0.460  -0.663  1.00  0.00           O  
HETATM    9  C7  UNL     1      -1.797  -0.514   1.352  1.00  0.00           C  
HETATM   10  C8  UNL     1      -3.144  -0.251   0.868  1.00  0.00           C  
HETATM   11  C9  UNL     1      -3.776  -1.219   0.115  1.00  0.00           C  
HETATM   12  C10 UNL     1      -5.063  -1.026  -0.376  1.00  0.00           C  
HETATM   13  C11 UNL     1      -5.718   0.138  -0.110  1.00  0.00           C  
HETATM   14  C12 UNL     1      -5.090   1.113   0.645  1.00  0.00           C  
HETATM   15  C13 UNL     1      -3.815   0.925   1.133  1.00  0.00           C  
HETATM   16  H1  UNL     1       3.897   1.978   0.787  1.00  0.00           H  
HETATM   17  H2  UNL     1       5.257   1.824  -0.452  1.00  0.00           H  
HETATM   18  H3  UNL     1       3.508   1.758  -0.955  1.00  0.00           H  
HETATM   19  H4  UNL     1       5.061  -0.277   0.699  1.00  0.00           H  
HETATM   20  H5  UNL     1       3.923  -0.173  -2.084  1.00  0.00           H  
HETATM   21  H6  UNL     1       3.658  -1.688  -1.074  1.00  0.00           H  
HETATM   22  H7  UNL     1       5.303  -1.067  -1.402  1.00  0.00           H  
HETATM   23  H8  UNL     1       2.991   0.204   1.789  1.00  0.00           H  
HETATM   24  H9  UNL     1       2.966  -1.420   1.060  1.00  0.00           H  
HETATM   25  H10 UNL     1       1.762   1.167  -0.080  1.00  0.00           H  
HETATM   26  H11 UNL     1       1.683  -0.380  -0.951  1.00  0.00           H  
HETATM   27  H12 UNL     1      -1.675  -1.611   1.514  1.00  0.00           H  
HETATM   28  H13 UNL     1      -1.673  -0.054   2.365  1.00  0.00           H  
HETATM   29  H14 UNL     1      -3.317  -2.170  -0.137  1.00  0.00           H  
HETATM   30  H15 UNL     1      -5.541  -1.807  -0.970  1.00  0.00           H  
HETATM   31  H16 UNL     1      -6.714   0.313  -0.478  1.00  0.00           H  
HETATM   32  H17 UNL     1      -5.642   2.018   0.832  1.00  0.00           H  
HETATM   33  H18 UNL     1      -3.377   1.723   1.716  1.00  0.00           H  
CONECT    1    2   16   17   18
CONECT    2    3    4   19
CONECT    3   20   21   22
CONECT    4    5   23   24
CONECT    5    6   25   26
CONECT    6    7
CONECT    7    8    8    9
CONECT    9   10   27   28
CONECT   10   11   11   15
CONECT   11   12   29
CONECT   12   13   13   30
CONECT   13   14   31
CONECT   14   15   15   32
CONECT   15   33
END

HMDB0035008
     RDKit          3D
3-Methylbutyl phenylacetate
 33 33  0  0  0  0  0  0  0  0999 V2000
    4.2375    1.4850   -0.1670 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2044    0.0090    0.0648 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2668   -0.7827   -1.2242 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9497   -0.3433    0.8289 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7008    0.0626    0.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5895   -0.3075    0.8439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7213   -0.0865    0.4428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8923    0.4600   -0.6633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7972   -0.5137    1.3523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1439   -0.2515    0.8684 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7760   -1.2189    0.1146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0634   -1.0264   -0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7180    0.1379   -0.1105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0903    1.1133    0.6452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8148    0.9251    1.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8970    1.9784    0.7869 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2567    1.8239   -0.4521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5077    1.7578   -0.9550 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0608   -0.2768    0.6995 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9231   -0.1734   -2.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6582   -1.6881   -1.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3026   -1.0667   -1.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9911    0.2042    1.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9661   -1.4199    1.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7620    1.1674   -0.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6831   -0.3802   -0.9506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6749   -1.6105    1.5145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6731   -0.0541    2.3648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3174   -2.1705   -0.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5413   -1.8070   -0.9698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7137    0.3125   -0.4775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6418    2.0182    0.8323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3774    1.7227    1.7162 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  9 27  1  0
  9 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  0
 15 33  1  0
M  END

Synonyms

Value	Source
3-Methylbutyl phenylacetic acid	Generator
3-Methylbutyl benzeneacetate	HMDB
Acetic acid, phenyl-, isopentyl ester	HMDB
Benzeneacetic acid, 3-methylbutyl ester	HMDB
FEMA 2081	HMDB
Isoamyl alpha-toluate	HMDB
Isoamyl phenylacetate	HMDB
Isopentyl alcohol, phenylacetate	HMDB
Isopentyl phenylacetate	HMDB
Isopentylphenylacetate	HMDB
Phenylacetic acid isoamyl ester	HMDB
Phenylacetic acid, 3-methylbutyl ester	HMDB
Phenylacetic acid, isopentyl ester	HMDB
3-Methylbutyl 2-phenylacetic acid	Generator

Molecular Formula

C₁₃H₁₈O₂

Average Mass

206.2808

Monoisotopic Mass

206.13067982

IUPAC Name

3-methylbutyl 2-phenylacetate

Traditional Name

3-methylbutyl 2-phenylacetate

CAS Registry Number

Not Available

SMILES

CC(C)CCOC(=O)CC1=CC=CC=C1

InChI Identifier

InChI=1S/C13H18O2/c1-11(2)8-9-15-13(14)10-12-6-4-3-5-7-12/h3-7,11H,8-10H2,1-2H3

InChI Key

QWBQBUWZZBUFHN-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Not Available

Direct Parent

Benzene and substituted derivatives

Alternative Parents

Substituents

Monocyclic benzene moiety
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.019 g/L	ALOGPS
logP	3.83	ALOGPS
logP	3.37	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Basic)	-7.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	60.56 m³·mol⁻¹	ChemAxon
Polarizability	24.05 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Biological Properties

Cellular Locations

Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces	Unknown

Exposure Sources

Food Exposures

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

HMDB0035008

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB013612

KNApSAcK ID

Not Available

Chemspider ID

7318

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

7600

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Robinson AL, Ebeler SE, Heymann H, Boss PK, Solomon PS, Trengove RD: Interactions between wine volatile compounds and grape and wine matrix components influence aroma compound headspace partitioning. J Agric Food Chem. 2009 Nov 11;57(21):10313-22. doi: 10.1021/jf902586n. [PubMed:19845354 ]
Yannai, Shmuel (2004). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. Boca Raton: Chapman & Hall/CRC..

Showing metabocard for Isoamyl phenylacetate (MMDBc0047711)

MOL for #<Metabolite:0x00007f1240d4fef0>

3D MOL for #<Metabolite:0x00007f1240d4fef0>

3D SDF for #<Metabolite:0x00007f1240d4fef0>

3D-SDF for #<Metabolite:0x00007f1240d4fef0>

PDB for #<Metabolite:0x00007f1240d4fef0>

3D PDB for #<Metabolite:0x00007f1240d4fef0>

SMILES for #<Metabolite:0x00007f1240d4fef0>

INCHI for #<Metabolite:0x00007f1240d4fef0>

Structure for #<Metabolite:0x00007f1240d4fef0>

3D Structure for #<Metabolite:0x00007f1240d4fef0>