1160293-75-3

Basic information

• Product Name: (3S)-2-[N-(2-nitrobenzenesulfonyl)amino]-3-(4-methoxyphenyl)propan-1-ol
• Synonyms: (3S)-2-[N-(2-nitrobenzenesulfonyl)amino]-3-(4-methoxyphenyl)propan-1-ol
• CAS NO: 1160293-75-3
• Molecular Weight: 366.395
• Mol File: 1160293-75-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3S)-2-[N-(2-nitrobenzenesulfonyl)amino]-3-(4-methoxyphenyl)propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (3S)-2-[N-(2-nitrobenzenesulfonyl)amino]-3-(4-methoxyphenyl)propan-1-ol(1160293-75-3)
• EPA Substance Registry System: (3S)-2-[N-(2-nitrobenzenesulfonyl)amino]-3-(4-methoxyphenyl)propan-1-ol(1160293-75-3)

Safety Data

• Hazardous Substances Data: 1160293-75-3(Hazardous Substances Data)

Upstream product

• 20989-22-4 (3S)-2-amino-3-(4-methoxyphenyl)propan-1-ol hydrochloride 
• 1694-92-4 2-Nitrobenzenesulfonyl chloride 
• 20401-88-1 3-(4-methoxyphenyl)propional 
• 6655-31-8 o-nitrobenzenesulfonyl azide 

Downstream Products

• 1160293-76-4 (3S)-2-[N-(2-nitrobenzenesulfonyl)-N-benzylamino]-3-(4-methoxyphenyl)propan-1-ol 

Relevant articles and documents

Enantioselective organocatalytic α-sulfamidation of aldehydes using sulfonyl azides

Enantioselective organocatalytic α-sulfamidation of unbranched aldehydes is described using MacMillan's second-generation imidazolidinone catalyst and o-nitrobenzenesulfonyl azide. The reactions are highly stereoselective (89.9–96.3% ee) with yields up to 71%. A strong correlation between aldehyde structure and product yield was found to exist, with 3-arylpropanals providing the best results. Application to functionalized amino acid synthesis is presented.