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Details

Stereochemistry ACHIRAL
Molecular Formula C9H10O
Molecular Weight 134.1751
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-PHENYLPROPIONALDEHYDE

SMILES

O=CCCC1=CC=CC=C1

InChI

InChIKey=YGCZTXZTJXYWCO-UHFFFAOYSA-N
InChI=1S/C9H10O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,8H,4,7H2

HIDE SMILES / InChI

Molecular Formula C9H10O
Molecular Weight 134.1751
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Importance of the nature of α-substituents in pyrrolidine organocatalysts in asymmetric Michael additions.
2010-11-05
Origin of pressure effects on regioselectivity and enantioselectivity in the rhodium-catalyzed hydroformylation of styrene with (S,S,S)-BisDiazaphos.
2010-08-04
Aminodifluorosulfinium salts: selective fluorination reagents with enhanced thermal stability and ease of handling.
2010-05-21
Phenylpropanoyl esters from Horseweed (Conyza canadensis) and their inhibitory effects on catecholamine secretion.
2010-02-26
Development of a novel catalytic membrane reactor for heterogeneous catalysis in supercritical CO₂.
2010-01-13
Taxomyces andreanae: a presumed paclitaxel producer demystified?
2009-12
Effect of mixed antimicrobial agents and flavors in active packaging films.
2009-09-23
Comparative analysis of 1-phenyl-2-propanone (P2P), an amphetamine-type stimulant precursor, using stable isotope ratio mass spectrometry: presented in part as a poster at the 2nd meeting of the Joint European Stable Isotope User Meeting (JESIUM), Giens, France, September 2008.
2009-06
Purification and characterization of aldehyde dehydrogenase with a broad substrate specificity originated from 2-phenylethanol-assimilating Brevibacterium sp. KU1309.
2007-08
Mechanistic and structural studies of apoform, binary, and ternary complexes of the Arabidopsis alkenal double bond reductase At5g16970.
2006-12-29
beta-Glucosidase inhibitory activities of phenylpropanoid glycosides, vanicoside A and B from Polygonum sachalinense rhizome.
2006-09
Pinus taeda phenylpropenal double-bond reductase: purification, cDNA cloning, heterologous expression in Escherichia coli, and subcellular localization in P. taeda.
2006-08
A type III polyketide synthase from Wachendorfia thyrsiflora and its role in diarylheptanoid and phenylphenalenone biosynthesis.
2006-07
Comparative analysis of volatile constituents from mice and their urine.
2006-06
Ultrasound-assisted hydrogenation of cinnamaldehyde.
2005-03
Strategy for the synthesis of polymeric supports with hydrazone linkers for solid-phase alkylation of ketones and aldehydes.
2005-01-11
Enantioselective catalysis of the hetero-Diels-Alder reaction between Brassard's diene and aldehydes by hydrogen-bonding activation: a one-step synthesis of (S)-(+)-dihydrokawain.
2004-11-19
Development of highly diastereo- and enantioselective direct asymmetric aldol reaction of a glycinate Schiff base with aldehydes catalyzed by chiral quaternary ammonium salts.
2004-08-11
Reversal of enantioselectivity in the hydroformylation of styrene with [2S,4S-BDPP]Pt(SnCl3)Cl at high temperature arises from a change in the enantioselective-determining step.
2004-05-05
Intramolecular electrophilic aromatic substitution in gas-phase-protonated difunctional compounds containing one or two arylmethyl groups.
2003-11
The arduous way to the egg: follow the nose.
2003-10-13
Catalytic asymmetric allylation of aldehydes and related reactions with bis(((S)-binaphthoxy)(isopropoxy)titanium) oxide as a mu-oxo-type chiral Lewis acid.
2003-09-22
N-acyl-5,5-dimethyloxazolidin-2-ones as latent aldehyde equivalents.
2003-06-07
Total synthesis of (+)-strictifolione.
2003-05-29
A novel potato defence-related alcohol:NADP+ oxidoreductase induced in response to Erwinia carotovora.
2003-05
Bis(((S)-binaphthoxy)(isopropoxy)titanium) oxide as a mu-oxo-type chiral Lewis acid: application to catalytic asymmetric allylation of aldehydes.
2003-02-19
Silanediol-based inhibitor of thermolysin.
2002-12-16
Thermolysis of alkyl sulfoxides and derivatives: a comparison of experiment and theory.
2001-12-28
Alpha-phenylethylamine in illegally produced amphetamine.
2001-12-01
High yield synthesis of nitriles by a new enzyme, phenylacetaldoxime dehydratase, from Bacillus sp. strain OxB-1.
2001-12
Determination of amphetamine and its metabolite p-hydroxyamphetamine in rat urine by reversed-phase high-performance liquid chromatography after dabsyl derivatization.
2001-11
Cornified envelope formation by anthralin, simple analogues, and related anthracenones.
2001-03
Structure-activity relationships of novel anti-malarial agents. Part 2: cinnamic acid derivatives.
2001-02-12
Enzymatic reduction of phenylproprionaldehyde.
2001
Suberin structure in potato periderm: glycerol, long-chain monomers, and glyceryl and feruloyl dimers.
2000-11
Antimicrobial intermediates of the general phenylpropanoid and lignin specific pathways.
2000-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:35:45 GMT 2025
Edited
by admin
on Mon Mar 31 18:35:45 GMT 2025
Record UNII
LP1E86N30T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-PHENYLPROPIONALDEHYDE
FCC   FHFI  
Systematic Name English
FEMA NO. 2887
Preferred Name English
PHENYLPROPYL ALDEHYDE
Common Name English
3-PHENYLPROPIONALDEHYDE [FCC]
Common Name English
BENZENEPROPANAL
Systematic Name English
3-PHENYL-1-PROPANAL
Systematic Name English
NSC-9271
Code English
BENZYLACETALDEHYDE
Systematic Name English
3-PHENYLPROPANAL
Systematic Name English
3-PHENYLPROPIONALDEHYDE [FHFI]
Common Name English
HYDROCINNAMALDEHYDE
Systematic Name English
PROPIONAIDEHYDE, 3-PHENYL-
Common Name English
.BETA.-PHENYLPROPIONALDEHYDE
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:35:45 GMT 2025 , Edited by admin on Mon Mar 31 18:35:45 GMT 2025
JECFA EVALUATION 3-PHENYLPROPIONALDEHYDE
Created by admin on Mon Mar 31 18:35:45 GMT 2025 , Edited by admin on Mon Mar 31 18:35:45 GMT 2025
Code System Code Type Description
ECHA (EC/EINECS)
203-211-8
Created by admin on Mon Mar 31 18:35:45 GMT 2025 , Edited by admin on Mon Mar 31 18:35:45 GMT 2025
PRIMARY
SMS_ID
100000172750
Created by admin on Mon Mar 31 18:35:45 GMT 2025 , Edited by admin on Mon Mar 31 18:35:45 GMT 2025
PRIMARY
CHEBI
39940
Created by admin on Mon Mar 31 18:35:45 GMT 2025 , Edited by admin on Mon Mar 31 18:35:45 GMT 2025
PRIMARY
EPA CompTox
DTXSID0047610
Created by admin on Mon Mar 31 18:35:45 GMT 2025 , Edited by admin on Mon Mar 31 18:35:45 GMT 2025
PRIMARY
NSC
9271
Created by admin on Mon Mar 31 18:35:45 GMT 2025 , Edited by admin on Mon Mar 31 18:35:45 GMT 2025
PRIMARY
WIKIPEDIA
Hydrocinnamaldehyde
Created by admin on Mon Mar 31 18:35:45 GMT 2025 , Edited by admin on Mon Mar 31 18:35:45 GMT 2025
PRIMARY
FDA UNII
LP1E86N30T
Created by admin on Mon Mar 31 18:35:45 GMT 2025 , Edited by admin on Mon Mar 31 18:35:45 GMT 2025
PRIMARY
CAS
104-53-0
Created by admin on Mon Mar 31 18:35:45 GMT 2025 , Edited by admin on Mon Mar 31 18:35:45 GMT 2025
PRIMARY
JECFA MONOGRAPH
689
Created by admin on Mon Mar 31 18:35:45 GMT 2025 , Edited by admin on Mon Mar 31 18:35:45 GMT 2025
PRIMARY
PUBCHEM
7707
Created by admin on Mon Mar 31 18:35:45 GMT 2025 , Edited by admin on Mon Mar 31 18:35:45 GMT 2025
PRIMARY