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B5151

Sigma-Aldrich

Benzil

98%

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Synonym(s):
Dibenzoyl, Diphenylethanedione
Linear Formula:
C6H5COCOC6H5
CAS Number:
Molecular Weight:
210.23
Beilstein:
608047
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

vapor pressure

1 mmHg ( 128.4 °C)

Assay

98%

form

crystals

mp

94-95 °C (lit.)

SMILES string

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

InChI

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

InChI key

WURBFLDFSFBTLW-UHFFFAOYSA-N

Gene Information

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

WGK

WGK 2

Flash Point(F)

356.0 °F

Flash Point(C)

180 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (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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