Skip to Content
Merck
All Photos(1)

Documents

E45309

Sigma-Aldrich

Ethyl phenylpropiolate

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H5C≡CCOOC2H5
CAS Number:
Molecular Weight:
174.20
Beilstein:
639637
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

liquid

refractive index

n20/D 1.552 (lit.)

bp

260-270 °C (lit.)

density

1.055 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CCOC(=O)C#Cc1ccccc1

InChI

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

InChI key

ACJOYTKWHPEIHW-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 5

1 of 5

Ethyl benzoylacetate technical grade, 90%

Sigma-Aldrich

281492

Ethyl benzoylacetate

Ethyl hydrocinnamate 99%

Sigma-Aldrich

284416

Ethyl hydrocinnamate

Methyl propiolate 99%

Sigma-Aldrich

171859

Methyl propiolate

4-Phenyl-3-butyn-2-ol 97%

Sigma-Aldrich

669288

4-Phenyl-3-butyn-2-ol

Cimetidine

Sigma-Aldrich

C4522

Cimetidine

Ampai Panthong et al.
Journal of ethnopharmacology, 91(2-3), 237-242 (2004-05-04)
Methanolic extracts from the heart wood, stem bark, and stem wood of Ventilago harmandiana Pierre (Family Rhamnaceae) were assessed for anti-inflammatory effects using both acute and chronic inflammatory models. Analgesic and antipyretic activities of the extracts were also evaluated. It
C McGaughey et al.
Journal of toxicology and environmental health, 11(3), 467-474 (1983-03-01)
Tumor initiation by topical application of 7,12-dimethylbenz[a]anthracene (DMBA) in dimethyl sulfoxide (DMSO) followed by topical application of retinyl acetate (RA), ethylphenylpropiolate, or acetic acid in DMSO at inflammatory and hyperplasiogenic dose regimens caused the rapid promotion of fibrovascular polyps with
P Claeson et al.
Planta medica, 62(3), 236-240 (1996-06-01)
The topical anti-inflammatory activity of three non-phenolic linear 1,7-diarylheptanoids, previously isolated from a Thai medicinal plant, Curcuma xanthorrhiza (Zingiberaceae) and four new semi-synthetic derivatives of the naturally occurring compounds were assessed in the murine model of ethyl phenylpropiolate-induced ear edema.
Tsugio Kitamura et al.
Nature protocols, 2(4), 845-848 (2007-04-21)
This protocol describes the synthesis of 6,7-methylenedioxy-4-phenylcoumarin from sesamol and ethyl phenylpropiolate using a Pd(OAc)2 catalyst to illustrate coumarin synthesis. This procedure is simple and easy and can be applied to the synthesis of other coumarins that have electron-rich phenol
K A Davidson et al.
The Journal of investigative dermatology, 79(6), 378-382 (1982-12-01)
Glucocorticoids (anti-inflammatory steroids) are very potent inhibitors of mouse skin tumor promotion induced by 12-O-tetradecanoylphorbol-13-acetate (TPA). This report describes a high-affinity, limited-capacity binding component which specifically interacts with glucocorticoids and which is identified as a glucocorticoid (GC) receptor present in

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service