97821-21-1

Basic information

• Product Name: isopropyl N-phenyl sulfinamoyl ester
• Synonyms: isopropyl N-phenyl sulfinamoyl ester
• CAS NO: 97821-21-1
• Molecular Weight: 183.274
• Mol File: 97821-21-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: isopropyl N-phenyl sulfinamoyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: isopropyl N-phenyl sulfinamoyl ester(97821-21-1)
• EPA Substance Registry System: isopropyl N-phenyl sulfinamoyl ester(97821-21-1)

Safety Data

• Hazardous Substances Data: 97821-21-1(Hazardous Substances Data)

Upstream product

• 1068-55-9 isopropylmagnesium chloride 
• 222851-56-1 N-phenylsulfinylamine 
• 62-53-3 aniline 
• 24053-95-0 N-phenyladamantane-1-sulfinamide 
• 34256-07-0 isopropylsulfinyl chloride 
• 133497-27-5 (±)-2-methyl-N-phenylpropane-2-sulfinamide 
• 52693-47-7 methyl i-propylsulfinate 
• 75-29-6 isopropyl chloride 

Downstream Products

• 60901-23-7 N-phenylpropane-2-sulfonamide 
• 133497-27-5 (±)-2-methyl-N-phenylpropane-2-sulfinamide 
• 73761-60-1 propane-2-sulfinic acid 
• 62-53-3 aniline 
• 1520120-20-0 3-[(anilinoisopropyloxo-1λ⁶-sulfanylidene)amino]propanoic acid 
• 1520119-93-0 ethyl 3-[(anilinoisopropyloxo-1λ⁶-sulfanylidene)amino]propanoate 
• 97773-46-1 ZnCl₂*2(N-phenyl 2-propane sulfinamide) 
• 97773-45-0 ZnBr₂*2(N-phenyl 2-propane sulfinamide) 

Relevant articles and documents

Synthesis of six-membered cyclic sulfonimidamides

A general synthetic route to six-membered cyclic N-aryl- and N-alkyl-substituted sulfonimidamides via an intramolecular ring closure of suitably functionalised acyclic sulfonimidamides is described. The structure of this new ring system was confirmed by v

Mild and general method for the synthesis of sulfonamides

Reaction of methyl sulfinates with lithium amides followed by 3-chloroperoxybenzoic acid oxidation of the resulting sulfinamides provides primary, secondary, and tertiary alkane-, arene-and heteroarenesulfonamides in high yields. This constitutes a mild and facile experimental protocol that avoids the use of hazardous, unstable, or volatile reagents and does not affect the configurational stability of the amines. Georg Thieme Verlag Stuttgart.