B33706
联苄
ReagentPlus®, 99%
别名:
1,2-二苯乙烷, 联甲苯
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线性分子式:
C6H5CH2CH2C6H5
化学文摘社编号:
分子量:
182.26
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-096-4
Beilstein/REAXYS Number:
508068
MDL number:
产品名称
联苄, ReagentPlus®, 99%
InChI key
QWUWMCYKGHVNAV-UHFFFAOYSA-N
InChI
1S/C14H14/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-10H,11-12H2
SMILES string
C(Cc1ccccc1)c2ccccc2
product line
ReagentPlus®
assay
99%
form
crystals
autoignition temp.
896 °F
bp
284 °C (lit.)
mp
50-53 °C (lit.)
density
1.014 g/mL at 25 °C (lit.)
Quality Level
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Application
联苄用于制备阻燃、高密度硬质聚氨酯泡沫。此外，它还可用于合成乙酰胆碱酯酶 (AChE) 和丁酰胆碱酯酶 (BuChE) 抑制剂。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
Flame?retardant and mechanical properties of high?density rigid polyurethane foams filled with decabrominated dipheny ethane and expandable graphite.
Ye L, et al.
Journal of Applied Polymer Science, 111(5), 2372-2380 (2009)
Design, synthesis, and biological evaluation of a new series of biphenyl/bibenzyl derivatives functioning as dual inhibitors of acetylcholinesterase and butyrylcholinesterase.
Wang D M, et al.
Molecules (Basel), 22(1), 172-172 (2017)
Evan G Buchanan et al.
The Journal of chemical physics, 138(6), 064308-064308 (2013-02-22)
The spectroscopy of two flexible hydrocarbons, 1,2-diphenylethane (DPE) and 2,2,2-paracyclophane (TCP) is presented, and a predictive theoretical model for describing the alkyl CH stretch region of these hydrocarbons is developed. Ultraviolet hole-burning spectroscopy identified two isomers of DPE and a
K H Fritzemeier et al.
European journal of biochemistry, 133(3), 545-550 (1983-07-01)
Hydroxy derivatives of 9,10-dihydrophenanthrenes, orchinol and hircinol, were isolated from bulbs of Orchidaceae which had been induced to accumulate phytoalexins. Incorporation of radioactive precursors, L-phenylalanine and various hydroxycinnamic acids, has been investigated by feeding experiments in vivo. m-Coumaric acid and
Kohei Hosoi et al.
Chemical communications (Cambridge, England), 47(30), 8632-8634 (2011-07-02)
Electron transfer behavior of 1,2-diphenyl-o-carborane was investigated by cyclic voltammetry (CV). In the presence of 1,2-dibromo-1,2-diphenylethane, a significant catalytic current was observed. The macroscale electrocatalytic reduction of the dibromide using a catalytic amount (1 mol%) of the carborane mediator afforded
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