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Details

Stereochemistry ACHIRAL
Molecular Formula C11H10O2
Molecular Weight 174.1959
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYL 3-PHENYLPROPYNOATE

SMILES

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

InChI

InChIKey=ACJOYTKWHPEIHW-UHFFFAOYSA-N
InChI=1S/C11H10O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-7H,2H2,1H3

HIDE SMILES / InChI

Molecular Formula C11H10O2
Molecular Weight 174.1959
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Anti-HIV-1 and anti-inflammatory lupanes from the leaves, twigs, and resin of Garcinia hanburyi.
2010-03
Anti-inflammatory, analgesic and wound healing activities of the leaves of Memecylon edule Roxb.
2009-01-21
Anti-inflammatory activity of gel containing novel elastic niosomes entrapped with diclofenac diethylammonium.
2008-08-06
Palladium-catalyzed hydroarylation of alkynes with arenediazonium salts.
2008-04-17
Platinum-catalyzed regio- and stereoselective arylthiolation of internal alkynes.
2008-01-03
Analgesic, anti-inflammatory and venotonic effects of Cissus quadrangularis Linn.
2007-03-21
Practical and convenient synthesis of coumarins from phenols and propiolic acid esters.
2007
Anti-inflammatory activity of methanolic extracts from Ventilago harmandiana Pierre.
2004-04
Anti-inflammatory activity of (E)-1-(3,4-dimethoxyphenyl) butadiene from Zingiber cassumunar Roxb.
2003-08
The analgesic, antipyretic and anti-inflammatory activity of Diospyros variegata Kruz.
2003-04
Models of acute inflammation in the ear.
2003
Anti-inflammatory and antioxidant properties of Helichrysum italicum.
2002-03
A mechanistic approach to the in vivo anti-inflammatory activity of sesquiterpenoid compounds isolated from Inula viscosa.
2001-11
Cytokine induction in human epidermal keratinocytes exposed to contact irritants and its relation to chemical-induced inflammation in mouse skin.
1994-06
Murine epidermal xanthine oxidase activity: correlation with degree of hyperplasia induced by tumor promoters.
1987-12-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:40:30 GMT 2025
Edited
by admin
on Mon Mar 31 19:40:30 GMT 2025
Record UNII
09CYB3Z9MR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-41566
Preferred Name English
ETHYL 3-PHENYLPROPYNOATE
Systematic Name English
ETHYL 3-PHENYL-2-PROPYNOATE
Systematic Name English
ETHYL 2-PHENYLACETYLENECARBOXYLATE
Systematic Name English
3-PHENYL-2-PROPYNOIC ACID ETHYL ESTER
Systematic Name English
ETHYL PHENYLPROPIOLATE
Systematic Name English
ETHYL PHENYLACETYLENECARBOXYLATE
Systematic Name English
PROPIOLIC ACID, PHENYL-, ETHYL ESTER
Systematic Name English
ETHYL PHENYLPROPYNOATE
Systematic Name English
ETHYL 3-PHENYLPROPARGYLATE
Common Name English
2-PROPYNOIC ACID, 3-PHENYL-, ETHYL ESTER
Systematic Name English
ETHYL 3-PHENYLPROPIOLATE
Systematic Name English
Code System Code Type Description
PUBCHEM
91516
Created by admin on Mon Mar 31 19:40:30 GMT 2025 , Edited by admin on Mon Mar 31 19:40:30 GMT 2025
PRIMARY
CAS
2216-94-6
Created by admin on Mon Mar 31 19:40:30 GMT 2025 , Edited by admin on Mon Mar 31 19:40:30 GMT 2025
PRIMARY
ECHA (EC/EINECS)
218-703-8
Created by admin on Mon Mar 31 19:40:30 GMT 2025 , Edited by admin on Mon Mar 31 19:40:30 GMT 2025
PRIMARY
NSC
41566
Created by admin on Mon Mar 31 19:40:30 GMT 2025 , Edited by admin on Mon Mar 31 19:40:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID9074858
Created by admin on Mon Mar 31 19:40:30 GMT 2025 , Edited by admin on Mon Mar 31 19:40:30 GMT 2025
PRIMARY
FDA UNII
09CYB3Z9MR
Created by admin on Mon Mar 31 19:40:30 GMT 2025 , Edited by admin on Mon Mar 31 19:40:30 GMT 2025
PRIMARY