119905-80-5

Basic information

• Product Name: 1,2,3-Cyclopentanetriol, 4-(hydroxymethyl)-, (1S,2R,3R,4R)-
• CAS NO: 119905-80-5
• Molecular Formula: C6H12O4
• Mol File: 119905-80-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1,2,3-Cyclopentanetriol, 4-(hydroxymethyl)-, (1S,2R,3R,4R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3-Cyclopentanetriol, 4-(hydroxymethyl)-, (1S,2R,3R,4R)-(119905-80-5)
• EPA Substance Registry System: 1,2,3-Cyclopentanetriol, 4-(hydroxymethyl)-, (1S,2R,3R,4R)-(119905-80-5)

Safety Data

• Hazardous Substances Data: 119905-80-5(Hazardous Substances Data)

Upstream product

• 119826-17-4 Benzoic acid (1R,2R,3R)-3-benzyloxy-2-formyloxy-4-hydroxy-5-nitro-cyclopentylmethyl ester 
• 119826-19-6 Benzoic acid (1R,2R,3R,4S)-2,4-diacetoxy-3-benzyloxy-cyclopentylmethyl ester 
• 119826-16-3 Benzoic acid (2R,3R,4S)-4-benzyloxy-3-formyloxy-2-nitromethyl-5-oxo-pentyl ester 
• 4594-60-9 methyl 3,4-O-isopropylidene-β-D-arabinopyranoside 
• 5328-63-2 methyl-β-D-arabinopyranoside 
• 28697-53-2 D-arabinopyranose 
• 178931-90-3 3,4,5-tri-O-benzyl-1,2,6-trideoxy-L-xylo-hex-1-enitol 
• 85716-43-4 methyl 6-deoxy-6-iodo-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 73111-16-7 3,4,5-tri-O-benzyl-1,2-dideoxy-L-xylo-hex-1-enitol 
• 921770-88-9 (1R,4S)-4-[(2S)-1,4-dioxaspiro[4.5]dec-2-yl]cyclopent-2-en-1-ol 
• 727428-98-0 (S)-(S)-5-(1,4-Dioxa-spiro[4.5]dec-2-yl)-hepta-1,6-dien-3-ol 
• 921770-99-2 (1R,2S,3R,4R)-2,3-bis(benzyloxy)-4-[(2S)-1,4-dioxaspiro[4.5]dec-2-yl]cyclopentanol 
• 921771-08-6 (S)-1-((1R,2R,3R,4S)-2,3,4-Tris-benzyloxy-cyclopentyl)-ethane-1,2-diol 
• 921771-00-8 (2R,3R,4R)-2,3-bis(benzyloxy)-4-[(2S)-1,4-dioxaspiro[4.5]dec-2-yl]cyclopentanone 

Relevant articles and documents

A convenient approach for access to both carbapentofuranoses and carbahexopyranoses. Stereocontrolled synthesis of enantiopure Carba-D-ribofuranoses, Carba-D-arabinofuranoses and Carba-L-gulopyranose

A new approach to carbasugars in enantiomerically pure form is reported. The key step involves ring-closing metathesis of dienols 6 derived from a (R)-(+)-glyceraldehyde derivative 4 to form the substituted cyclopentenol 9 and cyclohexenol 34a. Stereocont

Cobalt-catalysed radical oxygenation with molecular oxygen

Molecular oxygen is an efficient trap in cobalt-catalysed radical substitution and 5-exo radical cyclization reactions.

Samarium(II) Iodide Promoted Ring Contraction of Carbohydrate Derivatives: an Expeditious Synthesis of Functionalised Cyclopentanes

Aldehydo methyl pyranosides undergo ring contraction induced by treatment with samarium(ii) iodide, in the presence of HMPA and tert-butyl alcohol, to give highly functionalised cyclopentanes.