1015198-49-8

Basic information

• Product Name: 2-methylpropane-2-sulfinic acid [1-(2-methoxyphenyl)methylidene]amide
• Synonyms: 2-methylpropane-2-sulfinic acid [1-(2-methoxyphenyl)methylidene]amide
• CAS NO: 1015198-49-8
• Molecular Weight: 239.338
• Mol File: 1015198-49-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-methylpropane-2-sulfinic acid [1-(2-methoxyphenyl)methylidene]amide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methylpropane-2-sulfinic acid [1-(2-methoxyphenyl)methylidene]amide(1015198-49-8)
• EPA Substance Registry System: 2-methylpropane-2-sulfinic acid [1-(2-methoxyphenyl)methylidene]amide(1015198-49-8)

Safety Data

• Hazardous Substances Data: 1015198-49-8(Hazardous Substances Data)

Upstream product

• 135-02-4 ortho-anisaldehyde 
• 196929-78-9 (R)-2-methylpropane-2-sulfinamide 

Downstream Products

• 1187081-57-7 (R)-N-((S,E)-2-benzylidene-1-(2-methoxyphenyl)-4-phenylbut-3-ynyl)-2-methylpropane-2-sulfinamide 
• 1373313-73-5 (R)-N-((R)-1-(2-methoxyphenyl)but-3-enyl)-2-methylpropane-2-sulfinamide 
• 1272676-11-5 C₁₈H₂₉NO₄S 
• 1333259-58-7 C₁₃H₁₉F₂NO₂S 
• 1310082-59-7 C₁₄H₂₁NO₂S 
• 1015198-68-1 C₁₅H₂₃NO₂S 

Relevant articles and documents

Studies on diastereofacial selectivity of a chiral tert-butanesulfinimines for the preparation of (S)-3-Methyl-1-(2-piperidin-1-yl-phenyl)butylamine for the synthesis of repaglinide

A new method for the asymmetric synthesis of a series of chiral amines including (S)-3-methyl-1-(2-piperidin-1-yl-phenyl)butylamine (2a) a key intermediate to prepare antidiabetic drug repaglinide by using Ellman's reagent tert-butanesulfinamide. Diastereoselective addition of organometallic reagents to t-butanesulfinimines and followed by acidic and basic treatment. The obtained chiral amines were characterized by NMR, MS and other analytical data.