1036404-01-9

Basic information

• Product Name: (R)-(N-benzyloxycarbonyl)-2-(2-oxoethyl)pyrrolidine
• Synonyms: (R)-(N-benzyloxycarbonyl)-2-(2-oxoethyl)pyrrolidine
• CAS NO: 1036404-01-9
• Molecular Weight: 247.294
• Mol File: 1036404-01-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R)-(N-benzyloxycarbonyl)-2-(2-oxoethyl)pyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(N-benzyloxycarbonyl)-2-(2-oxoethyl)pyrrolidine(1036404-01-9)
• EPA Substance Registry System: (R)-(N-benzyloxycarbonyl)-2-(2-oxoethyl)pyrrolidine(1036404-01-9)

Safety Data

• Hazardous Substances Data: 1036404-01-9(Hazardous Substances Data)

Upstream product

• 72597-18-3 (2R)-(+)-phenylmethyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate 
• 50463-82-6 (2R)-(+)-phenylmethyl 2-formylpyrrolidine-1-carboxylate 
• 197230-34-5 (R)-2-allyl-(N-benzyloxycarbonyl) pyrrolidine 
• 1597449-88-1 (2R,Rs)-2-allyl-(N-tert-butylsulfinyl)pyrrolidine 
• 1597449-87-0 (4R,R_S)-N-(tert-butylsulfinyl)-7-bromohept-1-en-4-amine 
• 1000806-50-7 (E)-(6-benzyloxycarbonylamino)-2-hexenal 

Downstream Products

• 61350-64-9 (R)-2-{1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}acetic acid 
• 1597449-90-5 (2R,2′S,R_S)-(N-benzyloxycarbonyl)-2-[(2′-tert-butylsulfinamine)-4′-pentenyl]pyrrolidine 
• 1597449-89-2 (2R,2′R,S_S)-(N-benzyloxycarbonyl)-2-[2′-(tert-butylsulfinamine)-4′-pentenyl]pyrrolidine 

Relevant articles and documents

FUMAGILLOL HETEROCYCLIC COMPOUNDS AND METHODS OF MAKING AND USING SAME

Disclosed herein, in part, are fumagillol compounds and methods of use in treating medical disorders, such as obesity. Pharmaceutical compositions and methods of making fumagillol compounds are provided. The compounds are contemplated to have activity against methionyl aminopeptidase 2.

Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: Enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid

(Chemical Equation Presented) An improved protocol for the construction of enantioenriched pyrrolidine, indoline, and piperidine rings using an organocatalyzed, intramolecular heteroatom Michael addition is described. Application to the enantioselective synthesis of homoproline, homopipecolic acid, and pelletierine has been accomplished.