蒸汽压
1 mmHg ( 128.4 °C)
检测方案
98%
形式
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
WGK
WGK 2
闪点(°F)
356.0 °F
闪点(°C)
180 °C
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
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
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
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
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
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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