ETHYL PHENYLACETATE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C10H12O2
Molecular Weight	164.2011
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CCOC(=O)CC1=CC=CC=C1

InChI

InChIKey=DULCUDSUACXJJC-UHFFFAOYSA-N

InChI=1S/C10H12O2/c1-2-12-10(11)8-9-6-4-3-5-7-9/h3-7H,2,8H2,1H3

HIDE SMILES / InChI

Molecular Formula	C10H12O2
Molecular Weight	164.2011
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Classification of wines from five Spanish origin denominations by aromatic compound analysis.	2011-02-15	21313821
Branched-chain and aromatic amino acid catabolism into aroma volatiles in Cucumis melo L. fruit.	2010-02	20065117
The Ayurvedic drug, Ksheerabala, ameliorates quinolinic acid-induced oxidative stress in rat brain.	2010-01	20532090
Chemical Investigation of Crataeva nurvala Buch. Ham. Fruits.	2009-03	20336208
Linking gene regulation and the exo-metabolome: a comparative transcriptomics approach to identify genes that impact on the production of volatile aroma compounds in yeast.	2008-11-07	18990252
Characterization of the most odor-active compounds in an American Bourbon whisky by application of the aroma extract dilution analysis.	2008-07-23	18570373
Methanolysis of ethyl esters of N-acetyl amino acids catalyzed by cyclosophoraoses isolated from Rhizobium meliloti.	2008-02-04	18045579
An organocatalytic oxidative coupling strategy for the direct synthesis of arylated quaternary stereogenic centers.	2007-11-08	17924643
Sweet-like off-flavor in Aglianico del Vulture wine: ethyl phenylacetate as the mainly involved compound.	2007-06-27	17530858
Synthesis and biological evaluation of 1,3,3,4-tetrasubstituted pyrrolidine CCR5 receptor antagonists. Discovery of a potent and orally bioavailable anti-HIV agent.	2007-02	17163560
Phenolic constituents in the fruits of Cinnamomum zeylanicum and their antioxidant activity.	2006-03-08	16506818
Synthesis of 2H-1,2-benzothiazine 1,1-dioxides via heteroannulation reactions of 2-iodobenzenesulfonamide with ketone enolates under S(RN)1 conditions.	2005-11-11	16268584
Influence of volatile compounds produced by yeasts predominant during processing of Coffea arabica in East Africa on growth and ochratoxin A (OTA) production by Aspergillus ochraceus.	2005-10-30	16240461
Synthesis of ethyl phenylacetate by lyophilized mycelium of Aspergillus oryzae.	2005-06	15650849
Aerosolized essential oils and individual natural product compounds as brown treesnake repellents.	2002-08	12192901

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:49:11 GMT 2025` Edited by `admin` on `Mon Mar 31 18:49:11 GMT 2025`
Record UNII	V6CNZ04D8O
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

ETHYL PHENYLACETATE

Official Name

English

FEMA NO. 2452

Preferred Name

English

NSC-8894

Code

English

ETHYL PHENACETATE

Common Name

English

NSC-406259

Code

English

BENZENEACETIC ACID, ETHYL ESTER

Common Name

English

ETHYL 2-PHENYLETHANOATE

Systematic Name

English

ETHYL PHENYLACETATE [MI]

Common Name

English

ETHYL PHENYLACETATE [FHFI]

Common Name

English

ETHYL .ALPHA.-TOLUATE

Systematic Name

English

ETHYL PHENYLACETATE [FCC]

Common Name

English

ETHYL .ALPHA.-PHENYLACETATE

Systematic Name

English

ACETIC ACID, PHENYL-, ETHYL ESTER

Common Name

English

Ethylphenylacetate

Common Name

English

ETHYL BENZENEACETATE

Systematic Name

English

PHENYLACETIC ACID, ETHYL ESTER

Common Name

English

Classification Tree Code System Code

CFR

21 CFR 172.515