649552-54-5

Basic information

• Product Name: (R)-(-)-N-(hexanylidene)-p-toluenesulfinamide
• Synonyms: (R)-(-)-N-(hexanylidene)-p-toluenesulfinamide
• CAS NO: 649552-54-5
• Molecular Weight: 237.366
• Mol File: 649552-54-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-(-)-N-(hexanylidene)-p-toluenesulfinamide(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(-)-N-(hexanylidene)-p-toluenesulfinamide(649552-54-5)
• EPA Substance Registry System: (R)-(-)-N-(hexanylidene)-p-toluenesulfinamide(649552-54-5)

Safety Data

• Hazardous Substances Data: 649552-54-5(Hazardous Substances Data)

Upstream product

• 66-25-1 hexanal 
• 247089-85-6 (R)-p-toluenesulfinamide 

Downstream Products

• 1025936-50-8 (7S,8S,10R)-8-(3-Benzyloxy-propyl)-7-methyl-10-pentyl-1,5-dioxa-9-aza-spiro[5.5]undecane 
• 649552-57-8 (7S,8S,10R)-8-((E)-3-Benzyloxy-propenyl)-7-methyl-10-pentyl-1,5-dioxa-9-aza-spiro[5.5]undecane 
• 649552-56-7 (R)-(-)-1-(2-ethyl-1,3-dioxan-2-yl)-2-aminoheptane 
• 649552-55-6 (R_S,R)-(-)-N-(p-toluenesulfinyl)-5-amino-3-decanone 

Relevant articles and documents

Direct Asymmetric Synthesis of β-Amino Ketones from Sulfinimines (N-Sulfinylimines). Synthesis of (-)-Indolizidine 209B

(Equation presented) N-Sulfinyl β-amino ketones, prepared directly from the potassium enolates of methyl ketones and enantiopure sulfinimines, are transformed in one pot to protected amino ketones, which are valuable chiral building blocks for the assembl