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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
Alpha-phenylethylamine in illegally produced amphetamine.
2001 Dec 1
Bis(((S)-binaphthoxy)(isopropoxy)titanium) oxide as a mu-oxo-type chiral Lewis acid: application to catalytic asymmetric allylation of aldehydes.
2003 Feb 19
N-acyl-5,5-dimethyloxazolidin-2-ones as latent aldehyde equivalents.
2003 Jun 7
A novel potato defence-related alcohol:NADP+ oxidoreductase induced in response to Erwinia carotovora.
2003 May
Total synthesis of (+)-strictifolione.
2003 May 29
Intramolecular electrophilic aromatic substitution in gas-phase-protonated difunctional compounds containing one or two arylmethyl groups.
2003 Nov
The arduous way to the egg: follow the nose.
2003 Oct 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 Sep 22
Development of highly diastereo- and enantioselective direct asymmetric aldol reaction of a glycinate Schiff base with aldehydes catalyzed by chiral quaternary ammonium salts.
2004 Aug 11
Mechanistic and structural studies of apoform, binary, and ternary complexes of the Arabidopsis alkenal double bond reductase At5g16970.
2006 Dec 29
Purification and characterization of aldehyde dehydrogenase with a broad substrate specificity originated from 2-phenylethanol-assimilating Brevibacterium sp. KU1309.
2007 Aug
Taxomyces andreanae: a presumed paclitaxel producer demystified?
2009 Dec
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 Jun
Effect of mixed antimicrobial agents and flavors in active packaging films.
2009 Sep 23
Origin of pressure effects on regioselectivity and enantioselectivity in the rhodium-catalyzed hydroformylation of styrene with (S,S,S)-BisDiazaphos.
2010 Aug 4
Phenylpropanoyl esters from Horseweed (Conyza canadensis) and their inhibitory effects on catecholamine secretion.
2010 Feb 26
Development of a novel catalytic membrane reactor for heterogeneous catalysis in supercritical CO₂.
2010 Jan 13
Aminodifluorosulfinium salts: selective fluorination reagents with enhanced thermal stability and ease of handling.
2010 May 21
Importance of the nature of α-substituents in pyrrolidine organocatalysts in asymmetric Michael additions.
2010 Nov 5
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:45:45 GMT 2023
Edited
by admin
on Fri Dec 15 16:45:45 GMT 2023
Record UNII
LP1E86N30T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-PHENYLPROPIONALDEHYDE
FCC   FHFI  
Systematic Name English
PHENYLPROPYL ALDEHYDE
Common Name English
FEMA NO. 2887
Code 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 Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
JECFA EVALUATION 3-PHENYLPROPIONALDEHYDE
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
203-211-8
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
SMS_ID
100000172750
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
CHEBI
39940
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
EPA CompTox
DTXSID0047610
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
NSC
9271
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
WIKIPEDIA
Hydrocinnamaldehyde
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
FDA UNII
LP1E86N30T
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
CAS
104-53-0
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
JECFA MONOGRAPH
689
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
PUBCHEM
7707
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY