141774-67-6

Basic information

• Product Name: (S)-benzyl 2-(azidomethyl)pyrrolidine-1-carboxylate
• Synonyms: (S)-benzyl 2-(azidomethyl)pyrrolidine-1-carboxylate
• CAS NO: 141774-67-6
• Molecular Weight: 260.296
• Mol File: 141774-67-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (S)-benzyl 2-(azidomethyl)pyrrolidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-benzyl 2-(azidomethyl)pyrrolidine-1-carboxylate(141774-67-6)
• EPA Substance Registry System: (S)-benzyl 2-(azidomethyl)pyrrolidine-1-carboxylate(141774-67-6)

Safety Data

• Hazardous Substances Data: 141774-67-6(Hazardous Substances Data)

Upstream product

• 172885-53-9 (S)-2-iodomethyl-pyrrolidine-1-carboxylic acid benzyl ester 
• 6216-63-3 N-Cbz-Prolinol 
• 98-59-9 p-toluenesulfonyl chloride 
• 72500-24-4 (2S)-2-(4-methylphenylsulfonyloxymethyl)-pyrrolidine-1-carboxylic acid benzyl ester 

Downstream Products

• 944261-68-1 C₁₉H₂₂N₄O₆ 
• 1638689-33-4 C₁₆H₁₈N₄O₄ 
• 1474047-58-9 benzyl (S)-2-({(1S,2S,3R,5S)-2-[(tert-butoxycarbonyl)amino]-2,6,6-trimethylbicyclo[3.1.1]heptan-3-ylcarboxamido}methyl)pyrrolidine-1-carboxylate 
• 1321848-92-3 benzyl (S)-2-((3-(3,5-bis(trifluoromethyl)phenyl)thioureido)methyl)pyrrolidine-1-carboxylate 
• 1033749-63-1 C₂₀H₂₈N₄O₂ 
• 119020-03-0 2-(S)-aminomethyl-pyrrolidine-1-carboxylic acid benzyl ester 

Relevant articles and documents

Synthesis of Nα-Z protected amino alkyl triazole acids and their application to neo-glycopeptides synthesis

The synthesis of triazole linked glycopeptides employing 2-chloro-4,6-dimethoxy-1,3,5-triazine (CDMT) mediated coupling of Z-protected triazole acids with glycosyl amines and amino acid esters is described. The coupling proceeded smoothly at room temperat

Synthesis of chiral NADH analog based on proline template including thiourea and nicotinic acid moieties

Chiral reductase-mimicking organic molecule built on proline template incorporating a covalently bound NADH mimic via thiourea, and related reducing agent Hantzsch dihydropyridine, was designed. A synthetic path was developed involving interlinking of chiral proline derivatives with thiourea and subsequent coupling reaction with nicotinoyl chloride. The structure of target compound was studied by x-ray, indicating a double H bond with thiourea hydrogens and oxygen O1 of benzylcarbamate fragment. The reduction of benzil and imines was performed. Taylor & Francis Group, LLC.

Efficient synthesis of fused 1,2,3-triazolo-δ-lactams using Huisgen [3 + 2] dipolar cycloaddition "click-chemistry" in water

A general approach for the quick synthesis of various 1,2,3-triazolo- δ-lactams has been described, which involves the Huisgen [3 + 2] dipolar cycloaddition of azides derived from different amino acids with dimethyl acetylenedicarboxylate in water followe