Results for:
PubChem ID: 637520

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

Mass-Spectra

Compound Details

Synonymous names
Methyl cinnamate
103-26-4
Methyl trans-cinnamate
1754-62-7
Methyl (E)-cinnamate
Cinnamic acid methyl ester
Methyl (E)-3-phenylprop-2-enoate
Methyl 3-phenylpropenoate
Methyl cinnamylate
Methyl 3-phenylacrylate
Methylcinnamate
trans-Methyl cinnamate
(E)-Methyl cinnamate
Methyl trans-3-phenyl-2-propenoate
methyl-3-phenylprop-2-enoate
Methyl 3-phenyl-2-propenoate
FEMA No. 2698
methyl (2E)-3-phenylprop-2-enoate
trans-Cinnamic acid methyl ester
CINNAMIC ACID, METHYL ESTER
SemaSORB 9815
2-Propenoic acid, 3-phenyl-, methyl ester
2-propenoic acid, 3-phenyl-, methyl ester, (2E)-
Methyl (E)-3-phenyl-2-propenoate
2-PROPENOIC ACID, 3-PHENYL-, METHYL ESTER, (E)-
trans-Methyl 3-Phenyl-2-propenoate
Cinnamic acid, methyl ester, (E)-
(E)-3-Phenylacrylic acid methyl ester
533CV2ZCQL
methyl 3-phenylprop-2-enoate
CHEBI:6857
Methyl (2E)-3-phenylacrylate
Methyl (E)-3-phenylpropenoate
DTXSID5044314
NSC 9411
NSC-9411
MFCD00008458
Methyl cinnamate (natural)
cis-methyl cinnamate
Methyl cinnamate, (E)
EINECS 203-093-8
UNII-533CV2ZCQL
DTXSID6042151
AI3-00579
Methyl (2E)-3-phenyl-2-propenoate
3-Phenyl-2-propenoic acid methyl ester
Methyl(E)-cinnamate
methyl trans cinnamate
methyl-trans-cinnamate
EC 203-093-8
WLN: 1OV1U1R
ghl.PD_Mitscher_leg0.369
CHEMBL55060
Methyl trans-3-Phenylacrylate
Methyl trans-cinnamate, 99%
SCHEMBL101530
METHYL CINNAMATE [FCC]
(e)-cinnamic acid methyl ester
METHYL CINNAMATE [FHFI]
DTXCID4022151
DTXCID5028118
METHYL CINNAMATE, (E)-
Methyl (2E)-3-phenylpropenoate
NSC9411
3-Phenyl-2-propenoic acid methyl
CHEBI:194138
Tox21_301384
Tox21_304025
s6221
STL582416
Methyl cinnamate, >=99.0% (GC)
AKOS015890136
CS-W017928
HY-W017212
CINNAMIC ACID METHYL ESTER [MI]
Methyl (2E)-3-phenyl-2-propenoate #
trans-3-Phenylacrylic Acid Methyl Ester
NCGC00255910-01
NCGC00357235-01
CAS-103-26-4
DS-17838
LS-13765
CAS-1754-62-7
Methyl trans-cinnamate, analytical standard
Methyl trans-cinnamate, >=98%, FCC, FG
(E)-3-Phenyl-2-propenoic acid methyl ester
(E)-methyl ester 3-phenyl-2-propenoic acid
NS00001299
(2E)-3-Phenyl-2-propenoic acid methyl ester
EN300-91678
trans-3-Phenyl-2-propenoic acid methyl ester
C06358
EN300-365971
Methyl cinnamate, analytical reference material
Methyl cinnamate, natural, >=98%, FCC, FG
P16737
trans-3-phenyl-prop-2-enoic acid methyl ester
Q204178
J-000917
J-011115
J-522598
Q-100258
Z19782655
InChI=1/C10H10O2/c1-12-10(11)8-7-9-5-3-2-4-6-9/h2-8H,1H3/b8-7
Microorganism:

No

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
Molweight162.18
LogP2.6
Atoms12
Bonds3
H-bond Acceptor2
H-bond Donor0
Chemical Classificationaromatic compounds esters benzenoids
CHEBI-ID194138
Supernatural-IDSN0042129-01

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaFistulina Hepatican/aoak trees (October 2003 from Wisent Park, Springe)Wu et al. 2005
EukaryotaLentinus LepideusNABirkinshaw and Findlay 1940
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaFistulina Hepatican/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).no
EukaryotaLentinus Lepideusno