108227
苯甲酰苯胺
98%
别名:
N-苯基苯甲酰胺, N-苯甲酰替苯胺
质量水平
方案
98%
表单
solid
沸点
117 °C/10 mmHg (lit.)
mp
161-163 °C (lit.)
溶解性
H2O: insoluble
diethyl ether: slightly soluble
官能团
amide
phenyl
SMILES字符串
O=C(Nc1ccccc1)c2ccccc2
InChI
1S/C13H11NO/c15-13(11-7-3-1-4-8-11)14-12-9-5-2-6-10-12/h1-10H,(H,14,15)
InChI key
ZVSKZLHKADLHSD-UHFFFAOYSA-N
基因信息
human ... EPHX2(2053)
mouse ... Ephx2(13850)
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一般描述
苯甲酰苯胺在钯催化系统下与芳基三氟甲磺酸酯或溴化物发生二芳基化反应生成相应的的 N-（2,6-二芳基苯甲酰基）苯胺 。它用于制造染料和香水。
应用
用苯甲酰苯胺研究 β-环糊精对乙酰苯胺、苯甲酰苯胺和碳酸乙酯的光重排反应的影响 。它被用作酰胺模型化合物来研究酰胺与环氧化合物的反应 。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Dritan Hasa et al.
Pharmaceutics, 12(11) (2020-11-20)
Dodeca-2E,4E,8Z,10E/Z-tetraenoic isobutylamide (tetraene) is the main component of Echinacea angustifolia DC. lipophilic extract, the bioavailability and immunomodulatory effect after oral administration in soft gel capsules in healthy volunteers of which we have already demonstrated. In the present work, we assessed
Variable frequency microwave curing of amide-epoxy based polymers.
Tanaka K, et al.
IEEE Transactions on Components and Packaging Technologies, 30(3), 472-477 (2007)
Andrew K L Goey et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(1), 41-48 (2010-12-03)
Echinacea purpurea is one of the most popular herbal medicines and is known for its immunostimulatory effects. Alkylamides are the main lipophilic components of E. purpurea that contribute to its pharmacological actions. For quantification in human plasma of one of
Regioselective arylation of benzanilides with aryl triflates or bromides under palladium catalysis.
Kametani Y, et al.
Tetrahedron Letters, 41(15), 2655-2658 (2000)
Wan-Ping Hu et al.
Bioorganic & medicinal chemistry, 16(9), 5295-5302 (2008-03-25)
A series of novel thiobenzanilides is described. These compounds have been previously found to show strong biological activity such as antimycotic and antifungal actions. This is the first demonstration on the mechanism of the anticancer effect of thiobenzanilide agents (4a-c)
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