CAS 18303-04-3: N-(tert-butoxycarbonyl)-P-toluene-sulfonamide
Formula:C12H17NO4S
InChI:InChI=1/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)
SMILES:Cc1ccc(cc1)S(=O)(=O)N=C(O)OC(C)(C)C
Synonyms:- N-(tert-Butoxycarbonyl)-p-toluenesulfonamide
- Butoxycarbonyltoluenesulfonamide
- Tert-Butyl [(4-Methylphenyl)Sulfonyl]Carbamate
- N-BOC-Toluenesulfonamide
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Found 5 products.
N-(tert-Butoxycarbonyl)-p-toluenesulfonamide
CAS:Formula:C12H17NO4SPurity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:271.33tert-Butyl N-(4-methylphenyl)sulfonylcarbamate
CAS:tert-Butyl N-(4-methylphenyl)sulfonylcarbamatePurity:98+%Molecular weight:271.33g/molN-(tert-Butoxycarbonyl)-p-toluenesulfonamide
CAS:Purity:98.0%Color and Shape:SolidMolecular weight:271.3299865722656N-(tert-Butoxycarbonyl)-p-toluenesulfonamide
CAS:N-(tert-Butoxycarbonyl)-p-toluenesulfonamide is a compound that belongs to the class of organic compounds known as sulfonamides. It is the enantiopure form of the racemic mixture, which contains equal amounts of both enantiomers. N-(tert-Butoxycarbonyl)-p-toluenesulfonamide is an acidic compound and can be used in reactions involving halides, amines, and functional groups. The preparation of this compound involves ring-opening with alcohols or carboxylic acids, followed by reaction with ammonia. Impurities found in this compound include genotoxic impurities and vinylic impurities. N-(tert-Butoxycarbonyl)-p-toluenesulfonamide has been shown to have carbohydrate binding activity.Formula:C12H17NO4SPurity:Min. 95%Molecular weight:271.33 g/molRef: 3D-FB176115
Discontinued producttert-Butyl tosylcarbamate
CAS:Formula:C12H17NO4SPurity:95%Color and Shape:SolidMolecular weight:271.33268
