蒸汽压
1 mmHg ( 128.4 °C)
方案
98%
表单
crystals
mp
94-95 °C (lit.)
SMILES字符串
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
基因信息
human ... ACHE(43), BCHE(590), CES1(1066)
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警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
356.0 °F - closed cup
闪点(°C)
180 °C - closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
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
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
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
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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