232173
S,S-二苯基硫亚胺 一水合物
97%
登录查看公司和协议定价
选择尺寸
关于此项目
线性分子式:
(C6H5)2S=NH · H2O
化学文摘社编号:
分子量:
219.30
Beilstein:
2043848
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
方案
97%
表单
powder
mp
67-71 °C (lit.)
官能团
thioether
SMILES字符串
[H]O[H].N=S(c1ccccc1)c2ccccc2
InChI
1S/C12H11NS.H2O/c13-14(11-7-3-1-4-8-11)12-9-5-2-6-10-12;/h1-10,13H;1H2
InChI key
YLGYIQQZVOCMDO-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
一般描述
Kinetics and mechanism of reaction of S,S-diphenylsulfilimine with 1-fluoro-2,4-dinitrobenzene, 1-chloro-2,4-dinitrobenzene, 2-chloro-3-nitropyridine, 2-chloro-5-nitropyridine and 2-chloro-3,5-dinitropyridine has been investigated.
应用
S,S-Diphenylsulfilimine monohydrate is a versatile synthetic tool and has been used in preparation of:
- N-(5-nitrosouracil-6-yl)sulfilimines
- N-(1,3-dimethyl-6-uracilyl)-S,S-diphenylsulfilimines
- N-(5-formyl-1,3-dimethyl-6-uracilyl)-S,S-diphenylsulfilimines
储存分类代码
11 - Combustible Solids
WGK
WGK 3
Ring closure reactions of ?-nitroso-, ?-acyl-, and ?-thiocarbamoyl-a, ?-unsaturated sulfilimines. Synthesis of [1, 2, 5] oxadiazolo [3, 4-d]-, isoxazolo [3, 4-d]-, and isothiazolo [3, 4-d] pyrimidine derivatives from uracils.
Matsumoto N and Takahashi M.
Tetrahedron, 58(50), 10073-10079 (2002)
Kinetics and mechanism of the reaction of S, S-diphenylsulfilimine with a series of aryl halides.
Sandall JB and Steel ND.
J. Chem. Soc. Perkin Trans. II, 3, 513-516 (1997)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持