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Merck
CN

E45309

Ethyl phenylpropiolate

98%

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About This Item

Linear Formula:
C6H5C≡CCOOC2H5
CAS Number:
2216-94-6
Molecular Weight:
174.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24894561
EC Number:
218-703-8
Beilstein/REAXYS Number:
639637
MDL number:
MFCD00009185

Key Documents

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Product Name

Ethyl phenylpropiolate, 98%

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

SMILES string

CCOC(=O)C#Cc1ccccc1

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

Quality Level

100

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Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB1902
STBK5840
STBJ2546
STBH2949
S16570V

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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
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.
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
G S Cameron et al.
Cancer research, 51(20), 5642-5648 (1991-10-15)
The ability of the hyperplasiogenic irritant ethyl phenylpropiolate (EPP) to act as a tumor promoter in two-stage carcinogenesis and to stimulate cellular events commonly cited as markers of tumor promoter action was evaluated. Treatment of adult, inbred SENCAR (SSIN) mice
M Takigawa et al.
Cancer research, 46(1), 106-112 (1986-01-01)
More than one application of the potent tumor-promoting agent, 12-O-tetradecanoylphorbol-13-acetate (TPA), to mouse skin at intervals of more than 48 h led to a larger induction of ornithine decarboxylase (EC 4.1.1.17; ODC) than did a single application. In contrast, at
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