Results for:
PubChem ID: 637520

Methyl (E)-3-phenylprop-2-enoate

Mass-Spectra

Compound Details

Synonymous names
Methylcinnamate
CCRCUPLGCSFEDV-BQYQJAHWSA-N
Methyl cinnamylate
Methyl cinnamate
methyl-cinnamate
Benzeneacrylic acid methyl ester
methyl trans cinnamate
Methyl trans-cinnamate
trans-Methyl cinnamate
Cinnamic acid methyl
Methyl 3-phenylpropenoate
Methyl cinnamate, analytical reference material
Methyl 3-phenylacrylate
AC1LCUE5
AC1Q5YZH
Cinnamic acid methyl ester
Methyl trans-cinnamate, analytical standard
Methyl trans-3-Phenylacrylate
trans-Cinnamic acid methyl ester
Methyl 3-phenyl propenoate
Nat. Methyl Cinnamate
AC1Q41KG
533CV2ZCQL
CINNAMIC ACID, METHYL ESTER
Methyl cinnamate (natural)
PubChem8189
A517
trans-3-Phenylacrylic Acid Methyl Ester
CHEMBL55060
NSC9411
UNII-533CV2ZCQL
(E)-Methyl cinnamate
Methyl (E)-cinnamate
SemaSORB 9815
EBD44996
Methyl 3-phenyl-2-propenoate
methyl-3 phenylprop-2-enoate
methyl-3-phenylprop-2-enoate
RP17386
SCHEMBL101530
C06358
CHEBI:6857
Methyl trans-cinnamate, 99%
ZINC896129
AK312789
DTXSID5044314
LS-2916
Methyl (E)-3-phenylpropenoate
Methyl trans-3-phenyl-2-propenoate
NSC 9411
NSC-9411
OR025160
OR231744
SBB058222
TL806143
trans-Methyl 3-Phenyl-2-propenoate
WLN: 1OV1U1R
ZB015073
3-Phenyl-2-propenoic acid methyl
Methyl cinnamate, (E)
3-Phenyl-2-propenoic acid methyl ester
AJ-24225
AK-93451
AN-24625
DSSTox_GSID_44314
Methyl (2E)-3-phenylpropenoate
DSSTox_CID_22151
DSSTox_RID_80147
Methyl (2E)-3-phenylacrylate
MFCD00008458
ZINC00896129
AI3-00579
KB-203137
RTR-030565
ST24031190
ST50411952
TC-166123
TR-030565
trans-3-Phenyl-2-propenoic acid methyl ester
(E)-3-Phenylacrylic acid methyl ester
AKOS015890136
ghl.PD_Mitscher_leg0.369
I01-5731
I01-7774
J-000917
J-011115
J-522598
Q-100258
FEMA No. 2698
FT-0623832
Tox21_301384
103-26-4
Methyl (E)-3-phenyl-2-propenoate
Methyl (E)-3-phenylprop-2-enoate
1754-62-7
Methyl cinnamate, 99% 100g
Methyl trans-cinnamate, >=98%, FCC, FG
NCGC00255910-01
EINECS 203-093-8
methyl (2E)-3-phenylprop-2-enoate
Cinnamic acid, methyl ester, (E)-
Methyl 3-phenyl propenoate; 3-Phenyl-2-propenoic acid methyl ester
Methyl cinnamate, >=99.0% (GC)
(E)-3-Phenyl-2-propenoic acid methyl ester
CAS-1754-62-7
Methyl cinnamate, natural, >=98%, FCC, FG
403649-70-7
925685-28-5
Methyl (2E)-3-phenyl-2-propenoate #
(2E)-3-Phenyl-2-propenoic acid methyl ester
MolPort-001-783-139
MolPort-019-640-936
2-PROPENOIC ACID, 3-PHENYL-, METHYL ESTER, (E)-
2-propenoic acid, 3-phenyl-, methyl ester, (2E)-
InChI=1/C10H10O2/c1-12-10(11)8-7-9-5-3-2-4-6-9/h2-8H,1H3/b8-7
Microorganism:

Yes

IUPAC namemethyl (E)-3-phenylprop-2-enoate
SMILESCOC(=O)C=CC1=CC=CC=C1
InchiInChI=1S/C10H10O2/c1-12-10(11)8-7-9-5-3-2-4-6-9/h2-8H,1H3/b8-7+
FormulaC10H10O2
PubChem ID637520
Molweight162.188
LogP2.52
Atoms22
Bonds22
H-bond Acceptor1
H-bond Donor0
Chemical Classificationbenzenoids alkenes esters

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiFistulina Hepatica (Schaeffer: Fr.) Frn/aoak trees (October 2003 from Wisent Park, Springe)Wu et al., 2005
Fungi Lentius LepideusBirkinshaw and findlay 1940
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiFistulina Hepatica (Schaeffer: Fr.) Frn/aThe MVOCS from the fruiting bodies of wild Fistulina hepatica were investigated by high resolution GC-MS, using a polar phase ZB-WAX. F.hepatica were isolated by liquid liquid extraction (CLLE).
Fungi Lentius Lepideusno