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Merck
CN

B5151

苯偶酰

98%

别名:

联苯甲酰, 联苯酰

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线性分子式:
C6H5COCOC6H5
化学文摘社编号:
分子量:
210.23
EC Number:
205-157-0
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
608047
MDL number:
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产品名称

苯偶酰, 98%

InChI key

WURBFLDFSFBTLW-UHFFFAOYSA-N

InChI

1S/C14H10O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10H

SMILES string

O=C(c1ccccc1)C(=O)c2ccccc2

vapor pressure

1 mmHg ( 128.4 °C)

assay

98%

form

crystals

mp

94-95 °C (lit.)

Gene Information

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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

356.0 °F - closed cup

flash_point_c

180 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

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Anna Hoerder-Suabedissen et al.
Cerebral cortex (New York, N.Y. : 1991), 28(5), 1882-1897 (2018-02-27)
The thalamus receives input from 3 distinct cortical layers, but input from only 2 of these has been well characterized. We therefore investigated whether the third input, derived from layer 6b, is more similar to the projections from layer 6a
Zijia Li et al.
Advanced science (Weinheim, Baden-Wurttemberg, Germany), 6(6), 1802163-1802163 (2019-04-03)
Methoxy-functionalized triphenylamine-imidazole derivatives that can simultaneously work as hole transport materials (HTMs) and interface-modifiers are designed for high-performance and stable perovskite solar cells (PSCs). Satisfying the fundamental electrical and optical properties as HTMs of p-i-n planar PSCs, their energy levels
Tsuneomi Kawasaki et al.
Organic letters, 10(18), 4085-4088 (2008-08-30)
Chiral crystals of achiral benzils act as efficient chiral initiators of asymmetric autocatalysis to afford highly enantioenriched pyrimidyl alkanols whose absolute configurations depend upon the enantiomorph of the crystal used in conjunction with asymmetric autocatalysis with amplification of enantiomeric excess.
Jonathan L Sessler et al.
Organic letters, 10(1), 73-75 (2007-12-07)
The isolation and characterization of an intermediate from the benzil-cyanide reaction is reported. The use of this trapping chemistry to produce a chemical indicator for the cyanide anion is described. It relies on the synthesis and reaction of a pi-extended
Céline Mousset et al.
Bioorganic & medicinal chemistry letters, 18(11), 3266-3271 (2008-05-15)
A series of benzil derivatives related to combretastatin A-4 (CA-4) have been synthesized by oxidation of diarylalkynes promoted by PdI(2) in DMSO. Using this new protocol, 14 benzils were prepared in good to excellent yields and their biological activity has

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