1229277-96-6

Basic information

• Product Name: (2S)-2-[methyl-((1S)-1-phenylethyl)-carbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester
• Synonyms: (2S)-2-[methyl-((1S)-1-phenylethyl)-carbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester
• CAS NO: 1229277-96-6
• Molecular Weight: 332.443
• Mol File: 1229277-96-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S)-2-[methyl-((1S)-1-phenylethyl)-carbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-2-[methyl-((1S)-1-phenylethyl)-carbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester(1229277-96-6)
• EPA Substance Registry System: (2S)-2-[methyl-((1S)-1-phenylethyl)-carbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester(1229277-96-6)

Safety Data

• Hazardous Substances Data: 1229277-96-6(Hazardous Substances Data)

Upstream product

• 135339-67-2 (2S)-2-[((1S)-1-phenylethyl)carbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 74-88-4 methyl iodide 

Downstream Products

• 1229278-02-7 (2S)-pyrrolidine-2-carboxylic acid N-methyl-N-((1S)-1-phenyl-ethyl)-amide 

Relevant articles and documents

Structure-reactivity relationships of l-proline derived spirolactams and α-methyl prolinamide organocatalysts in the asymmetric Michael addition reaction of aldehydes to nitroolefins

l-Proline derived spirolactams and α-methyl prolinamides act as organocatalysts for the asymmetric conjugate addition of aldehydes to nitroolefins in excellent yields, with good diastereoselectivity and enantioselectivity. Furthermore, low catalyst loadings (5 mol %) and a low aldehyde molar excess (1.5 M equiv) were achieved.