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Merck
모든 사진(1)

주요 문서

521175

Sigma-Aldrich

4-Ethynylbiphenyl

97%

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About This Item

Linear Formula:
C6H5C6H4C≡CH
CAS Number:
Molecular Weight:
178.23
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

97%

mp

88-91 °C (lit.)

작용기

phenyl

SMILES string

C#Cc1ccc(cc1)-c2ccccc2

InChI

1S/C14H10/c1-2-12-8-10-14(11-9-12)13-6-4-3-5-7-13/h1,3-11H

InChI key

BPBNKCIVWFCMJY-UHFFFAOYSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

Hitoshi Fukuda et al.
The Japanese journal of antibiotics, 55(3), 270-280 (2002-08-30)
Convulsant activity of pazufloxacin mesilate (PZFX mesilate), a new quinolone antibacterial agent for intravenous use, in combination with nonsteroidal anti-inflammatory drug (NSAID) was investigated in mice after intravenous or intracerebroventricular administration. Following results were obtained. 1. In combination with 4-biphenylacetic
Cu-Promoted Oxidative Trifluoromethylation of Terminal Alkynes with Difluoromethylene Phosphobetaine.
Deng X, et al.
Chin. J. Chem., 32(8), 689-693 (2014)
Shift of the acetylenic hydrogen during chemical and enzymatic oxidation of the biphenylacetylene triple bond.
P R Ortiz de Montellano et al.
Archives of biochemistry and biophysics, 209(2), 710-712 (1981-07-01)
Synthesis, Structures, and Excited-State Geometries of Alkynylgold (I) Complexes.
Gao L, et al.
European Journal of Inorganic Chemistry, 18, 2711-2719 (2009)
A Wade et al.
The Biochemical journal, 184(3), 509-517 (1979-12-15)
1. 4-Ethynylbiphenyl undergoes extensive metabolism in the rat and the rabbit, involving aromatic hydroxylation and oxidation of the ethynyl group. No metabolites containing the intact ethynyl group were detected. 2. In the rat unchanged 4-ethynylbiphenyl was concentrated initially in the

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