210345-08-7

Basic information

• Product Name: L-Proline, 5-(2-propenyl)-, methyl ester, (5R)- (9CI)
• Synonyms: L-Proline, 5-(2-propenyl)-, methyl ester, (5R)- (9CI);5-(2-(5R)-Propen-1-yl)-L-proline methyl ester;5-(2-Propenyl)L-(5R)-proline methyl ester
• CAS NO: 210345-08-7
• Molecular Formula: C₉H₁₅NO₂
• Molecular Weight: 169.2209
• Product Categories: PYRROLE
• Mol File: 210345-08-7.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: L-Proline, 5-(2-propenyl)-, methyl ester, (5R)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: L-Proline, 5-(2-propenyl)-, methyl ester, (5R)- (9CI)(210345-08-7)
• EPA Substance Registry System: L-Proline, 5-(2-propenyl)-, methyl ester, (5R)- (9CI)(210345-08-7)

Safety Data

• Hazardous Substances Data: 210345-08-7(Hazardous Substances Data)

Upstream product

• 59936-29-7 (S)-N-(tert-butoxycarbonyl)proline methyl ester 
• 762-72-1 allyl-trimethyl-silane 
• 188015-51-2 (2S,5R)-5-allylpyrrolidine-1,2-dicarboxylic acid 2-methyl ester 1-tert-butyl ester 
• 195964-65-9 (2S)-5-allyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 
• 108963-96-8 (S)-1-tert-butoxycarbonyl-5-methoxycarbonyl-pyrrolidin-2-one 
• 195964-54-6 1-tert-butyl 2-methyl (2S)-5-methoxypyrrolidine-1,2-dicarboxylate 
• 4931-66-2 methyl (S)-pyroglutamate 
• 98-79-3 L-Pyroglutamic acid 

Downstream Products

• 210345-12-3 (2S,5R)-5-Allyl-1-(2-benzyloxy-3-phenyl-pent-4-enoyl)-pyrrolidine-2-carboxylic acid methyl ester 
• 123457-52-3 (2S,5R)-5-allylpyrrolidine-1,2-dicarboxylic acid 1-benzylester 2-methylester 

Relevant articles and documents

Synthesis of novel unsaturated bicyclic lactams by ring-closing metathesis

An efficient and versatile synthetic method for the preparation of novel unsaturated fused bicyclic lactams is described. The crucial step of the stereoselective approach is the ting-closing metathesis reaction. The 6,5-, 7,5- and 8,5-fused 1-aza-2-oxobicycloalkenes can be obtained in five steps and good overall yield.

Synthesis of hydrophobic phase-tagged prolyl peptides featuring rapid reaction/separation

Hydrophobically tagged prolyl peptides were synthesized using an electrochemically modified prolyl moiety. The hydrophobic tag served a useful handle for the repetitive reaction/separation steps during solution-phase peptide synthesis. Furthermore, the ta

Synthesis of new bicyclic lactam peptidomimetics by ring-closing metathesis reactions

An efficient and versatile synthetic method for the preparation of new fused bicyclic lactams 3a and 3b is described. The spirane cyclopentane nucleus was easily installed by diallylation of the pyroglutamate derivative 18 followed by ring-closing metathe