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Plant-Associated Volatile Organic Compound (VOC) Database (PVD)

A database supporting research and application of VOCs produced by plants and plant-associated microbes

(E)-3-phenylprop-2-enal

Metabolic Pathways

map00940
map01060
map01100
map01110
map04750

Structure

IUPAC Name

(E)-3-phenylprop-2-enal

PubChem CID

637511

Synonymous Names

cinnamaldehyde
trans-Cinnamaldehyde
104-55-2
14371-10-9
Cinnamic aldehyde
3-Phenylacrylaldehyde
Cinnamal
(E)-Cinnamaldehyde
Zimtaldehyde
(2E)-3-phenylprop-2-enal
3-Phenylpropenal
2-Propenal, 3-phenyl-
Phenylacrolein
trans-Cinnamic aldehyde
Cinnamylaldehyde
(E)-3-Phenylpropenal
(E)-3-phenylprop-2-enal
(E)-3-Phenyl-2-propenal
Cassia aldehyde
3-Phenylacrolein
2-propenal, 3-phenyl-, (2E)-
3-phenylprop-2-enal
3-Phenyl-2-propenal
Cinnemaldehyde
Cinnamyl aldehyde
Abion CA
Cinnamaldehyde, (E)-
trans-Cinnamylaldehyde
Benzylideneacetaldehyde
beta-Phenylcrolein
3-Phenyl-2-propenaldehyde
Acrolein, 3-phenyl-
3-Fenylpropenal
FEMA No. 2286
3-Phenyl-2-propen-1-al
trans-3-Phenyl-2-propenal
(E)-Cinnamic aldehyde
NCI-C56111
2-Propenal, 3-phenyl-, (E)-
(2E)-3-phenylacrylaldehyde
.beta.-phenylacrolein
CHEBI:16731
Cinnamaldehyde, trans-
(E)-3-Phenyl-propenal
MFCD00007000
NSC-16935
NSC-40346
SR60A3XG0F
(3E)-3-phenylprop-2-enal
(2E)-3-Phenyl-2-propenal
CHEMBL293492
Aldehyd skoricovy
DTXSID6024834
XC-800
NCGC00091512-04
NSC 16935
WLN: VH1U1R
DTXCID504834
3-phenyl-propenal
Caswell No. 221A
FEMA Number 2286
3-Fenylpropenal [Czech]
Aldehyd skoricovy [Czech]
Cinnamic aldehyde (natural)
Hefty Dog and Cat Repellent
CAS-14371-10-9
CCRIS 3189
CCRIS 6222
Cinnamaldehyde [NF]
HSDB 209
EINECS 203-213-9
UNII-SR60A3XG0F
DTXSID1024835
EPA Pesticide Chemical Code 040506
BRN 0605737
BRN 1071571
e-cinnamaldehyde
AI3-00473
AI3-33275
transcinnamaldehyde
|A-Phenylacrolein
trans cinnamaldehyde
CNMA
(trans)-cinnamaldehyde
trans cinnamic aldehyde
trans-3-Phenylacrolein
CINNAMAL [INCI]
trans-3-phenyl-propenal
(E)-phenylvinyl aldehyde
(E)-3-phenylacrylaldehyde
bmse010257
Epitope ID:150921
CINNAMALDEHYDE [II]
CINNAMALDEHYDE [MI]
EC 203-213-9
trans-3-Phenylacrylaldehyde
Trans-Cinnamaldehyde ,(S)
SCHEMBL3441
trans-Cinnamaldehyde, 99%
(E)-3-phenyl-acrylaldehyde
CINNAMALDEHYDE [FCC]
trans-Cinnamaldehyde; trans-3-Phenylacrylaldehyde
Cinnamaldehyde (trans), neat
CINNAMALDEHYDE [FHFI]
CINNAMALDEHYDE [HSDB]
2-07-00-00273 (Beilstein Handbook Reference)
4-07-00-00984 (Beilstein Handbook Reference)
MLS002454394
CINNAMALDEHYDE (TRANS)
trans-Cinnamaldehyde, >=99%
DTXCID904835
GTPL2423
(E)-cinnamaldehyde (incorrect)
CINNAMALDEHYDE [USP-RS]
CINNAMALDEHYDE [WHO-DD]
trans-cinnamaldehyde (incorrect)
CHEBI:142921
HMS2268O08
HMS3885E04
HY-N0609
NSC16935
NSC40346
Tox21_111144
Tox21_200272
Tox21_201804
Tox21_303271
BDBM50203065
s3763
STK397371
AKOS000119171
Cinnamaldehyde, natural, >=95%, FG
CCG-266119
DB14184
Cinnamaldehyde min. 98%, for synthesis
Cinnamaldehyde 100 microg/mL in Toluene
NCGC00091512-01
NCGC00091512-02
NCGC00091512-05
NCGC00091512-06
NCGC00091512-07
NCGC00257017-01
NCGC00257826-01
NCGC00259353-01
trans-Cinnamaldehyde, analytical standard
AS-12078
AS-75456
CAS-104-55-2
SMR000112334
trans-Cinnamaldehyde, >=98%, FCC, FG
(E)-3-phenyl-2-propenal(E)-cinnamaldehyde
AM20060482
CS-0009609
EN300-19160
A14480
C00903
Cinnamaldehyde, Vetec(TM) reagent grade, 93%
D72477
EN300-735819
A801001
Q204036
W-205597
B99DD6C7-1C6D-4FE3-A172-54BFDB987683
Z3219847383
CINNAMALDEHYDE (CONSTITUENT OF CINNAMOMUM VERUM BARK) [DSC]
Cinnamaldehyde, United States Pharmacopeia (USP) Reference Standard
InChI=1/C9H8O/c10-8-4-7-9-5-2-1-3-6-9/h1-8H/b7-4
TRANS-CINNAMALDEHYDE (CONSTITUENT OF CINNAMOMUM CASSIA BARK) [DSC]

Formula

C9H8O

Molecular Weight

132.16

Chemical Class

Benzenoid, Aldehyde, Aromatic

Reference Link

González-Mas, M. C., Rambla, J. L., López-Gresa, M. P., Blázquez, M. A., and Granell, A. 2019. Volatile Compounds in Citrus Essential Oils: A Comprehensive Review. Front Plant Sci. 10:12.

Plants/Microbial Species and Abiotic/Biotic Stimuli

Plant/Microbial Species	Abiotic/Biotic Stimuli
Citrus paradisi (Grapefruit)	None

Confirmed/Hypothesized Functions