56439-58-8

Basic information

• Product Name: 2-Pyrrolidinemethanol, 1-benzoyl-, benzoate (ester), (2S)-
• CAS NO: 56439-58-8
• Molecular Formula: C19H19NO3
• Molecular Weight: 309.365
• Mol File: 56439-58-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Pyrrolidinemethanol, 1-benzoyl-, benzoate (ester), (2S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pyrrolidinemethanol, 1-benzoyl-, benzoate (ester), (2S)-(56439-58-8)
• EPA Substance Registry System: 2-Pyrrolidinemethanol, 1-benzoyl-, benzoate (ester), (2S)-(56439-58-8)

Safety Data

• Hazardous Substances Data: 56439-58-8(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 23356-96-9 (S)-1-Pyrrolidin-2-yl-methanol 
• 652970-42-8 (2S,4S)-(1-benzoyl-4-phenylselenopyrrolidin-2-yl)methyl benzoate 
• 652970-36-0 methyl (2S,4S)-1-benzoyl-4-phenylselenopyrrolidine-2-carboxylate 
• 51-35-4 4R-4-hydroxyproline 
• 31560-21-1 methyl (2S,4R)-1-benzoyl-4-(p-toluenesulfonyloxy)pyrrolidine-2-carboxylate 
• 31560-20-0 (2S,4R)-1-benzoyl-4-hydroxypyrrolidine-2-carboxylic acid methyl ester 
• 1499-56-5 (R)-4-hydroxy-L-proline ethyl ester 
• 72351-42-9 [2-(hydroxymethyl)-1-pyrrolidinyl](phenyl)methanone 
• 652970-43-9 (2S)-(1-benzoyl-3-pyrrolin-2-yl)methyl benzoate 
• 179116-00-8 (S)-2-(chloromethyl)pyrrolidine 

Downstream Products

• 65950-13-2 (S)-(2-(hydroxymethyl)pyrrolidin-1-yl)(phenyl)methanone 

Relevant articles and documents

PYRAZOLE DERIVATIVE

A compound represented by Formula (I): wherein Ar1 represents Formula (II): Ar2 represents a 5- or 6-membered aromatic heterocyclic group which may be substituted; and X represents Formula (III): a salt thereof, or a solvate of the compound or the salt. A potent platelet aggregation suppressant which does not inhibit COX-1 and COX-2 is provided.

Kinetic resolution of vic-amino alcohols catalyzed by a chiral Cu(II) complex

Kinetic resolution of N-benzoylated vic-amino alcohols was achieved by benzoylation in the presence of copper triflate and (R,R)-Ph-BOX as catalysts. The observed enantioselectivity was moderate to high. The method was applied to a kinetic resolution of r