D204803
二苯基乙炔
98%
别名:
二苯乙炔
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线性分子式:
C6H5C≡CC6H5
化学文摘社编号:
分子量:
178.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-926-6
Beilstein/REAXYS Number:
606478
MDL number:
产品名称
二苯基乙炔, 98%
InChI
1S/C14H10/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-10H
InChI key
JRXXLCKWQFKACW-UHFFFAOYSA-N
SMILES string
c1ccc(cc1)C#Cc2ccccc2
assay
98%
form
crystals
bp
170 °C/19 mmHg (lit.)
mp
59-61 °C (lit.)
density
0.99 g/mL at 25 °C (lit.)
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Anion-dependent switching: dynamically controlling the conformation of hydrogen-bonded diphenylacetylenes.
Ian M Jones et al.
Angewandte Chemie (International ed. in English), 50(20), 4597-4600 (2011-04-16)
Neola F McKinley et al.
The Journal of organic chemistry, 71(25), 9552-9555 (2006-12-02)
Carbolithiation of diphenylacetylene can be exploited to generate (E)-1-lithio-1,2-diphenylalkyl-1-enes which can be reacted in situ with triisopropylborate to stereoselectively provide (E)-1,2-diphenyl-1-alkylene boronic acids. These tetrasubstituted vinylboronic acids served as versatile intermediates for the generation of tetrasubstituted olefins with retention of
Dai Nishimura et al.
The Journal of organic chemistry, 73(7), 2496-2502 (2008-03-14)
Novel [2]rotaxanes bearing alpha-cyclodextrin (alpha-CD) derivatives and a diphenylacetylene axis molecule with trinitrobenzene as a bulky stopper have been prepared to investigate the relative rotary movement of a ring relative to an axis molecule and that of an axis molecule
Akihiro Yokoyama et al.
Organic letters, 10(15), 3207-3210 (2008-06-28)
Base-promoted self-condensation reactions of trans-stilbene and diphenylacetylene monomers bearing 4-alkylamino and 4'-methoxycarbonyl groups were investigated. Reactions of N-propyl monomers under pseudohigh-dilution conditions (a THF solution of monomer was added dropwise to a THF solution of LiHMDS) afforded the corresponding cyclic
Kazuki Tainaka et al.
The journal of physical chemistry. B, 114(45), 14657-14663 (2010-06-01)
DNA-mediated charge transfer has recently received a substantial attention because of its biological relevance in the DNA damage and DNA repair as well as the potential applications to nanoscale electronic devices. In contrast to the numerous mechanistic studies on oxidative
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