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521175

Sigma-Aldrich

4-Ethynylbiphenyl

97%

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About This Item

Fórmula linear:
C6H5C6H4C≡CH
Número CAS:
29079-00-3
Peso molecular:
178.23
Número MDL:
MFCD00102191
Código UNSPSC:
12352100
ID de substância PubChem:
24874192
NACRES:
NA.22

Ensaio

97%

pf

88-91 °C (lit.)

grupo funcional

phenyl

cadeia de caracteres SMILES

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

chave InChI

BPBNKCIVWFCMJY-UHFFFAOYSA-N

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
MKCC7974
MKBT3272V
MKBR2781V
48196PJV
48196PJ

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Cu-Promoted Oxidative Trifluoromethylation of Terminal Alkynes with Difluoromethylene Phosphobetaine.
Deng X, et al.
Chin. J. Chem., 32(8), 689-693 (2014)
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
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)
A Wade et al.
The Biochemical journal, 188(3), 867-872 (1980-06-15)
1. The metabolism of 4-ethynylbiphenyl has been studied in vitro with subcellular fractions of normal and induced rat liver, and rat intestinal microflora (caecal contents). 2. Oxidation was NADPH-dependent, was inhibited by CO and stimulated by pretreatment with phenobarbitone or
Rajneesh Misra et al.
Dalton transactions (Cambridge, England : 2003), 43(12), 4854-4861 (2014-02-01)
A series of meso arylethynyl BODIPYs (2a-2h) were designed and synthesized by the Pd-catalyzed Sonogashira cross-coupling reaction. The effects of the donor on the photophysical properties of the BODIPYs were explored. The DFT optimized structures and crystal structures show the
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