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5 G
$327.00
About This Item
线性分子式:
C6H5C6H4C≡CH
CAS号:
分子量:
178.23
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
97%
mp
88-91 °C (lit.)
官能团
phenyl
SMILES字符串
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
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
其他客户在看
Branched polyphenylenes by repetitive Diels-Alder cycloaddition.
Shifrina ZB, et al.
Macromolecules, 33(10), 3525-3529 (2000)
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
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
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)
相关内容
The terminal alkyne functionality has a wide range of applications including most recently the synthesis of spiropyran substituted 2,3-dicyanopyrazines and (±)-asteriscanolide, as well as conversion to enamines using resin-bound 2° amines.
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