产品名称

英文名称：N-(tert-Butoxycarbonyl)-p-toluenesulfonamide

同义词

18303-04-3、N-(tert-Butoxycarbonyl)-p-toluenesulfonamide、tert-Butyl tosylcarbamate、N-Boc-p-toluenesulfonamide、tert-butyl N-(4-methylphenyl)sulfonylcarbamate、MFCD00134267、Carbamic acid, [(4-methylphenyl)sulfonyl]-, 1,1-dimethylethyl ester、N-Boc-4-tolylsulfo、N-Boc-对甲苯磺酰胺

产品性质

CAS编号：18303-04-3

分子式：C12H17NO4S

分子量：271.33

MDL号：MFCD00134267

PubChem编号：688170

别名：N-Boc-对甲苯磺酰胺

英文别名：18303-04-3|N-(tert-Butoxycarbonyl)-p-toluenesulfonamide|tert-Butyl tosylcarbamate|N-Boc-p-toluenesulfonamide|tert-butyl N-(4-methylphenyl)sulfonylcarbamate|MFCD00134267|Carbamic acid, [(4-methylphenyl)sulfonyl]-, 1,1-dimethylethyl ester|N-Boc-4-tolylsulfo

规格或纯度：>98.0%

英文名称：N-(tert-Butoxycarbonyl)-p-toluenesulfonamide

运输条件：常规运输

产品介绍：在 Mitsunobu 条件下可直接与伯醇、仲醇和烯丙醇发生偶联反应生成各种磺酰基保护胺。N-(tert-Butoxycarbonyl)-p-toluenesulfonamide may be used in the preparation of enyne amide, precursor for Pauson-Khand reaction.N-(tert-Butoxycarbonyl)-p-toluenesulfonamide is a N-substituted sulphonamide and its reaction with N-trityl L-serine esters under Mitsunobu reaction conditions is reported. It can be directly coupled with primary, secondary and allylic alcohols under Mitsunobu conditions to afford various sulfonyl-protected amines.N-(tert-Butoxycarbonyl)-p-toluenesulfonamide may be used in the preparation of enyne amide, precursor for Pauson-Khand reaction.

PubChem SID：488191090

IUPAC Name：tert-butyl N-(4-methylphenyl)sulfonylcarbamate

INCHI：InChI=1S/C12H17NO4S/c1-9-5-7-10(8-6-9)18(15,16)13-11(14)17-12(2,3)4/h5-8H,1-4H3,(H,13,14)

InChi Key：DUTLOVSBVBGNDM-UHFFFAOYSA-N

Canonical SMILES：CC1=CC=C(C=C1)S(=O)(=O)NC(=O)OC(C)(C)C

Isomeric SMILES：CC1=CC=C(C=C1)S(=O)(=O)NC(=O)OC(C)(C)C

WGK Germany：3

PubChem CID：688170

Reaxy-Rn：2858665

熔点：121-123°C

产品包装