B5151
Benzil
98%
Synonym(s):
Dibenzoyl, Diphenylethanedione
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About This Item
Linear Formula:
C6H5COCOC6H5
CAS Number:
Molecular Weight:
210.23
Beilstein:
608047
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
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
human ... ACHE(43) , BCHE(590) , CES1(1066)
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
356.0 °F - closed cup
Flash Point(C)
180 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
Patrick A Julien et al.
Beilstein journal of organic chemistry, 13, 2160-2168 (2017-11-09)
We provide the first in situ and real-time study of the effect of milling frequency on the course of a mechanochemical organic reaction conducted using a vibratory shaker (mixer) ball mill. The use of in situ Raman spectroscopy for real-time
Sulagna Mukherjee et al.
Applied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme, 44(10), 1089-1098 (2019-02-27)
The role of carboxylesterase 3 (Ces3) in the lipolysis of adipocytes has been overlooked, as 2 major lipolytic enzymes, hormone-sensitive lipase and adipose triglyceride lipase, play more powerful roles in lipolysis. In this study, we explored the effects of Ces3
Dong-Gyu Cho et al.
Journal of the American Chemical Society, 130(36), 12163-12167 (2008-08-14)
The benzil-cyanide reaction is a cyanide-specific reaction that has been exploited to produce a colorimetric indicator for this toxic anion. This was done by producing a pi-extended analogue of benzil, 7, which is soluble in a 70:30 (v/v) mixture of
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.
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