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B33706

Sigma-Aldrich

Bibenzyl

ReagentPlus®, 99%

Sinonimo/i:

1,2-Diphenylethane, Dibenzyl

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About This Item

Formula condensata:
C6H5CH2CH2C6H5
Numero CAS:
103-29-7
Peso molecolare:
182.26
Beilstein:
508068
Numero CE:
203-096-4
Numero MDL:
MFCD00004796
Codice UNSPSC:
12352100
ID PubChem:
24891710
NACRES:
NA.22

Nome Commerciale

ReagentPlus®

Saggio

99%

Forma fisica

crystals

Temp. autoaccensione

896 °F

P. eboll.

284 °C (lit.)

Punto di fusione

50-53 °C (lit.)

Densità

1.014 g/mL at 25 °C (lit.)

Stringa SMILE

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
QWUWMCYKGHVNAV-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

Bibenzyl is used in the preparation of flame-retardant, high-density rigid polyurethane foams. Additionally, it can also be used to synthesize acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) inhibitors.

Note legali

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

230.0 °F - closed cup

Punto d’infiammabilità (°C)

110 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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meso-1,2-Dibromo-1,2-diphenylethane ≥97%

Sigma-Aldrich

106550

meso-1,2-Dibromo-1,2-diphenylethane

Methylsulfonylmethane Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1346

Methylsulfonylmethane

guaiacylglycerol-beta-guaiacyl ether AldrichCPR

Sigma-Aldrich

CDS013307

guaiacylglycerol-beta-guaiacyl ether

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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