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质量水平
方案
97%
表单
solid
mp
38-42 °C (lit.)
官能团
chloro
isothiocyanate
储存温度
2-8°C
SMILES字符串
Clc1cccc(Cl)c1N=C=S
InChI
1S/C7H3Cl2NS/c8-5-2-1-3-6(9)7(5)10-4-11/h1-3H
InChI key
SUCGVQHNGIQXGD-UHFFFAOYSA-N
一般描述
2,6-Dichlorophenyl isothiocyanate is an isothiocyanate derivative. It has been synthesized by using 2,6-dichlorobenzaldehyde oxime as a starting reagent.
应用
2,6-Dichlorophenyl isothiocyanate may be used as a precursor to synthesize 1-(2-aminoethyl)-2-cyano-3-(2,6-dichlorophenyl)guanidine.
警示用语:
Danger
危险声明
危险分类
Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
J W Tilley et al.
Journal of medicinal chemistry, 23(12), 1438-1439 (1980-12-01)
Starting with 2,6-dichlorophenyl isothiocyanate, 1-(2-aminoethyl)-2-cyano-3-(2,6-dichlorophenyl)guanidine (2) was prepared in three steps. In contrast to the corresponding thiourea 1, this compound was essentially inactive as an antihypertensive agent.
Birsa ML, et al.
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 222-222 (2014)
Fazila Rizvi et al.
Scientific reports, 9(1), 6738-6738 (2019-05-03)
A library of thiosemicarbazide derivatives of isoniazid 3-27, was synthesized and evaluated for their anti-inflammatory and urease inhibition activities, by using in vitro bioassays. Among these compounds 9, 10, 12, 21, and 26 were identified as new derivatives. Prolonged use
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