方案
97%
表单
liquid
折射率
n20/D 1.584 (lit.)
沸点
239 °C (lit.)
密度
1.169 g/mL at 25 °C (lit.)
SMILES字符串
CNc1ccc(Cl)cc1
InChI
1S/C7H8ClN/c1-9-7-4-2-6(8)3-5-7/h2-5,9H,1H3
InChI key
XCEYKKJMLOFDSS-UHFFFAOYSA-N
警示用语：
Danger
危险分类
Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3 - STOT SE 3
靶器官
Respiratory system
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
125.6 °F - closed cup
闪点(°C)
52 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
M Weiner et al.
Drug metabolism and disposition: the biological fate of chemicals, 8(3), 139-142 (1980-05-01)
Hepatic metabolism of aniline, p-chloro-N-methylaniline, and aminopyrine was determined in control male, New Zealand White rabbits or those bearing VX2 carcinoma (a prostaglandin-secreting tumor). In addition, the levels of cyclic AMP and cyclic GMP in the liver and the concentration
C Varshneya et al.
Toxicology letters, 31(2), 107-111 (1986-05-01)
White leghorn cockerels were fed a diet containing 0, 400, 800 and 1600 ppm of malathion for 90 days. Malathion O,O-dimethyl S-(1,2-dicarbethoxy) ethyl phosphorodithioate) at 800 and 1600 ppm caused a significant decrease in body weights. There was a significant
Brian W Budzik et al.
Bioorganic & medicinal chemistry letters, 20(4), 1363-1367 (2010-01-26)
A series of 3-aryl-4-isoxazolecarboxamides identified from a high-throughput screening campaign as novel, potent agonists of the human TGR5 G-protein-coupled receptor is described. Many analogues were readily accessible via solution-phase synthesis which resulted in the rapid identification of key structure-activity relationships
S Cottrell et al.
Xenobiotica; the fate of foreign compounds in biological systems, 20(7), 711-726 (1990-07-01)
1. Because of the low concentration of cytochrome P-450 in avocado fruit, microsomal fractions were prepared using polyethylene glycol aggregation and low-speed centrifugation, thus avoiding the need for high-speed centrifugation of large volumes of post-mitochondrial supernatant. Recoveries of cytochrome P-450
A Usha Rani et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(5), 1523-1529 (2010-03-20)
In this work, the vibrational spectral analysis was carried out by using FT-IR and FT-Raman spectroscopy in the range 400-4000 and 50-3500cm(-1) respectively, for the title molecule. The structural and spectroscopic data of the molecule in the ground state were
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