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Merck

B33706

Sigma-Aldrich

联苄

ReagentPlus®, 99%

别名:

1,2-二苯乙烷, 联甲苯

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About This Item

线性分子式:
C6H5CH2CH2C6H5
CAS号:
分子量:
182.26
Beilstein:
508068
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

產品線

ReagentPlus®

化驗

99%

形狀

crystals

自燃溫度

896 °F

bp

284 °C (lit.)

mp

50-53 °C (lit.)

密度

1.014 g/mL at 25 °C (lit.)

SMILES 字串

C(Cc1ccccc1)c2ccccc2

InChI

1S/C14H14/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-10H,11-12H2

InChI 密鑰

QWUWMCYKGHVNAV-UHFFFAOYSA-N

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應用

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。

法律資訊

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

230.0 °F - closed cup

閃點(°C)

110 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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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)
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)
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
Adelfo Reyes-Ramírez et al.
European journal of medicinal chemistry, 46(7), 2699-2708 (2011-04-26)
Several analogs of gigantol (1) were synthesized to evaluate their effect on the complexes Ca(2+)-calmodulin (CaM) and Ca(2+)-CaM-CaM sensitive phosphodiesterase 1 (PDE1). The compounds belong to four structural groups including, 1,2-diphenylethanes (2-11), diphenylmethanes (13-15), 1,3-diphenylpropenones (16-18), and 1,3-diphenylpropanes (20-22). In
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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