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B33706

Sigma-Aldrich

Bibenzyl

ReagentPlus®, 99%

Sinónimos:

1,2-Diphenylethane, Dibenzyl

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About This Item

Fórmula lineal:
C6H5CH2CH2C6H5
Número de CAS:
103-29-7
Peso molecular:
182.26
Beilstein/REAXYS Number:
508068
EC Number:
203-096-4
MDL number:
MFCD00004796
UNSPSC Code:
12352100
PubChem Substance ID:
24891710
NACRES:
NA.22

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.)

SMILES string

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 key

QWUWMCYKGHVNAV-UHFFFAOYSA-N

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Categorías relacionadas

Application

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.

Legal Information

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
STBJ9892
STBH6120
STBF1990V
STBB7583V
STBC0794V

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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)
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
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
Geunhyeong Jo et al.
Magnetic resonance in chemistry : MRC, 49(6), 374-377 (2011-04-01)
Resveratrol is a polyphenol isolated from many natural sources including grapes, mulberries, eucalyptus, spruce, lilies, and peanuts. The hydroxyl groups in polyphenols can be substituted with various functional groups, allowing production of multiple derivatives. NMR spectroscopy is used to identify
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