188183-29-1

Basic information

• Product Name: (2RS)-(1S,2R,4R)-10-(Dicyclohexylsulfamoyl)isobornyl 3-methyl-2-cyanobutanoate
• Synonyms: (2RS)-(1S,2R,4R)-10-(Dicyclohexylsulfamoyl)isobornyl 3-methyl-2-cyanobutanoate
• CAS NO: 188183-29-1
• Molecular Weight: 506.75
• Mol File: 188183-29-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2RS)-(1S,2R,4R)-10-(Dicyclohexylsulfamoyl)isobornyl 3-methyl-2-cyanobutanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (2RS)-(1S,2R,4R)-10-(Dicyclohexylsulfamoyl)isobornyl 3-methyl-2-cyanobutanoate(188183-29-1)
• EPA Substance Registry System: (2RS)-(1S,2R,4R)-10-(Dicyclohexylsulfamoyl)isobornyl 3-methyl-2-cyanobutanoate(188183-29-1)

Safety Data

• Hazardous Substances Data: 188183-29-1(Hazardous Substances Data)

Upstream product

• 22426-27-3 2-Cyano-3-methylbutanoic acid 
• 98134-33-9 2-Cyano-3-methylbutanoyl chloride 
• 96303-88-7 (-)-10-dicyclohexylsulfamoyl-D-isoborneol 

Downstream Products

• 154520-28-2 (2R)-(1S,2R,4R)-10-(Dicyclohexylsulfamoyl)isobornyl 2-(aminomethyl)-2-benzyl-3-methylbutanoate 
• 154520-27-1 (2R)-(1S,2R,4R)-10-(Dicyclohexylsulfamoyl)isobornyl 2-(aminomethyl)-2-isopropylpentanoate 
• 154520-26-0 (2R)-(1S,2R,4R)-10-(Dicyclohexylsulfamoyl)isobornyl 2-(aminomethyl)-2,3-dimethylbutanoate 
• 154520-37-3 (3R)-3-Isopropyl-3-propyl-2-azetidinone 
• 173914-48-2 (2R)-(1S,2R,4R)-10-dicyclohexylsulfamoylisobornyl 2-amino-2-aminomethyl-3-methylbutanoate 
• 154520-17-9 (2R)-(1S,2R,4R)-10-(Dicyclohexylsulfamoyl)isobornyl 2-cyano-2-isopropyl-4-pentenoate 
• 173914-44-8 (2R)-(1S,2R,4R)-10-dicyclohexylsulfamoylisobornyl 2-amino-2-cyano-3-methylbutanoate 
• 154520-16-8 (2R)-(1S,2R,4R)-10-(Dicyclohexylsulfamoyl)isobornyl 2-cyano-2,3-dimethylbutanoate 
• 143100-08-7 (1S,2R,4R)-10-dicyclohexylsulfamoylisobornyl (S)-3-phenyl-2-isopropyl-2-cyanopropanoate 
• 143100-09-8 (1S,2R,4R)-10-dicyclohexylsulfamoylisobornyl (R)-3-phenyl-2-isopropyl-2-cyanopropanoate 

Relevant articles and documents

Stereoselective Amination of Chiral Enolates: Synthesis of enantiomerically pure α,β-Diamino Acids, Chiral Key Compounds in the Synthesis of Conformationally Constrained Peptido- and Non-peptidomimetics

This work describes an efficient synthesis of enantiomerically pure (R)-2-aminomethylalanine, (R)-2-aminomethylnorvaline, (R)-2-aminomethylvaline, (R)-2-aminomethylleucine and (R)-2-aminomethylphenylalanine by electrophilic amination of chiral 2-cyanoeste