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
Aerosolized essential oils and individual natural product compounds as brown treesnake repellents.	2002 Aug	12192901
Synthesis of ethyl phenylacetate by lyophilized mycelium of Aspergillus oryzae.	2005 Jun	15650849
Synthesis of 2H-1,2-benzothiazine 1,1-dioxides via heteroannulation reactions of 2-iodobenzenesulfonamide with ketone enolates under S(RN)1 conditions.	2005 Nov 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 Oct 30	16240461
Phenolic constituents in the fruits of Cinnamomum zeylanicum and their antioxidant activity.	2006 Mar 8	16506818
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 Feb	17163560
Sweet-like off-flavor in Aglianico del Vulture wine: ethyl phenylacetate as the mainly involved compound.	2007 Jun 27	17530858
An organocatalytic oxidative coupling strategy for the direct synthesis of arylated quaternary stereogenic centers.	2007 Nov 8	17924643
Methanolysis of ethyl esters of N-acetyl amino acids catalyzed by cyclosophoraoses isolated from Rhizobium meliloti.	2008 Feb 4	18045579
Characterization of the most odor-active compounds in an American Bourbon whisky by application of the aroma extract dilution analysis.	2008 Jul 23	18570373
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 Nov 7	18990252
Chemical Investigation of Crataeva nurvala Buch. Ham. Fruits.	2009 Mar	20336208
Branched-chain and aromatic amino acid catabolism into aroma volatiles in Cucumis melo L. fruit.	2010 Feb	20065117
The Ayurvedic drug, Ksheerabala, ameliorates quinolinic acid-induced oxidative stress in rat brain.	2010 Jan	20532090
Classification of wines from five Spanish origin denominations by aromatic compound analysis.	2010 Nov-Dec	21313821

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 17:36:23 GMT 2023` Edited by `admin` on `Fri Dec 15 17:36:23 GMT 2023`
Record UNII	V6CNZ04D8O
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

ETHYL PHENYLACETATE

Official Name

English

NSC-8894

Code

English

ETHYL PHENACETATE

Common Name

English

ETHYL PHENYLACETATE [INCI]

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

FEMA NO. 2452

Code

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