228422-24-0

Basic information

• Product Name: Cyclopentanecarboxamide, 2-(hydroxymethyl)-, (1S,2R)- (9CI)
• Synonyms: Cyclopentanecarboxamide, 2-(hydroxymethyl)-, (1S,2R)- (9CI)
• CAS NO: 228422-24-0
• Molecular Formula: C7H13NO2
• Molecular Weight: 143.18362
• Product Categories: AMIDE
• Mol File: 228422-24-0.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Cyclopentanecarboxamide, 2-(hydroxymethyl)-, (1S,2R)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopentanecarboxamide, 2-(hydroxymethyl)-, (1S,2R)- (9CI)(228422-24-0)
• EPA Substance Registry System: Cyclopentanecarboxamide, 2-(hydroxymethyl)-, (1S,2R)- (9CI)(228422-24-0)

Safety Data

• Hazardous Substances Data: 228422-24-0(Hazardous Substances Data)

Upstream product

• 113428-55-0 hexahydro-cyclopenta[c]furan-1-one 
• 75658-84-3 (1S,5R)-3-oxabicyclo[3.3.0]octan-2-one 
• 3205-94-5 1-cyclopentene-1,2-dicarboxylic anhydride 

Downstream Products

• 4492-47-1 (+/-)-cis-2-(hydroxymethyl)cyclopentylamine 

Relevant articles and documents

Precursors for the production of chiral 1,3-aminoalcohols

The disclosure describes novel precursors for the preparation of chiral 1,3-aminoalcohols. The precursors are chiral 4-hydroxycarboxamides, 4-hydroxyhydroxamic acids, or 4-hydroxyhydrazides produced from chiral gamma-lactones, which in turn are derived from 1,4-diols by stereoselective oxidation. The chiral 4-hydroxycarboxamides, 4-hydroxyhydroxamic acids, or 4-hydroxyhydrazides are converted into chiral 1,3-aminoalcohols by stereospecific rearrangement.