1407543-93-4

Basic information

• Product Name: (S)-benzyl 2-((3'-amino-[2,2'-bipyridin]-3-yl)carbamoyl)pyrrolidine-1-carboxylate
• Synonyms: (S)-benzyl 2-((3'-amino-[2,2'-bipyridin]-3-yl)carbamoyl)pyrrolidine-1-carboxylate
• CAS NO: 1407543-93-4
• Molecular Weight: 417.467
• Mol File: 1407543-93-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-benzyl 2-((3'-amino-[2,2'-bipyridin]-3-yl)carbamoyl)pyrrolidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-benzyl 2-((3'-amino-[2,2'-bipyridin]-3-yl)carbamoyl)pyrrolidine-1-carboxylate(1407543-93-4)
• EPA Substance Registry System: (S)-benzyl 2-((3'-amino-[2,2'-bipyridin]-3-yl)carbamoyl)pyrrolidine-1-carboxylate(1407543-93-4)

Safety Data

• Hazardous Substances Data: 1407543-93-4(Hazardous Substances Data)

Upstream product

• 1024-94-8 3,3’-dinitro-2,2’-bipyridine 
• 75449-26-2 2,2'-bipyridine-3,3'-diamine 
• 1148-11-4 N-Benzyloxycarbonyl-L-proline 
• 5470-18-8 2-Chloro-3-nitropyridine 

Downstream Products

• 1407543-86-5 (S)-benzyl 2-((3'-((S)-pyrrolidine-2-carboxamido)-[2,2'-bipyridin]-3-yl)carbamoyl)pyrrolidine-1-carboxylate 
• 1407543-94-5 (S)-benzyl 2-((3'-((S)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxamido)-[2,2'-bipyridin]-3-yl)carbamoyl)pyrrolidine-1-carboxylate 
• 1407543-95-6 (S)-benzyl 2-((3'-(2-(benzyloxy)benzamido)-[2,2'-bipyridin]-3-yl)carbamoyl)pyrrolidine-1-carboxylate 
• 1407543-87-6 (S)-N-(3'-(2-hydroxybenzamido)-[2,2'-bipyridin]-3-yl)pyrrolidine-2-carboxamide 
• 1407543-96-7 (S)-benzyl 2-((3'-(4-methylbenzamido)-[2,2'-bipyridin]-3-yl)carbamoyl)pyrrolidine-1-carboxylate 
• 1407543-88-7 (S)-N-(3'-(4-methylbenzamido)-[2,2'-bipyridin]-3-yl)pyrrolidine-2-carboxamide 

Relevant articles and documents

Novel axially unfixed biaryl-based water-compatible organocatalysts: Design, synthesis and their asymmetric catalysis in direct aldol reactions in water

A family of novel axially unfixed biaryl-based, water-compatible bifunctional organocatalysts were designed and synthesized for asymmetric catalytic direct aldol reactions in water. These organocatalysts are comprised of prolinamide, aromatic sulfonamide and biaryl motifs. Under the optimal reaction conditions, one organocatalyst in particular delivered excellent stereocontrol (up to 99% ee and 99:1 dr) in direct aldol reactions of cyclohexanone with a variety of aromatic aldehydes in water. Georg Thieme Verlag Stuttgart, New York.