124575-13-9

Basic information

• Product Name: cis-4-p-toluenesulfonylaminocyclopent-2-enylmethanol
• Synonyms: cis-4-p-toluenesulfonylaminocyclopent-2-enylmethanol
• CAS NO: 124575-13-9
• Molecular Weight: 267.349
• Mol File: 124575-13-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: cis-4-p-toluenesulfonylaminocyclopent-2-enylmethanol(CAS DataBase Reference)
• NIST Chemistry Reference: cis-4-p-toluenesulfonylaminocyclopent-2-enylmethanol(124575-13-9)
• EPA Substance Registry System: cis-4-p-toluenesulfonylaminocyclopent-2-enylmethanol(124575-13-9)

Safety Data

• Hazardous Substances Data: 124575-13-9(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 49805-30-3 2-azabicyclo[2.2.1.]hept-5-en-3-one 
• 542-92-7 cyclopenta-1,3-diene 
• 49805-30-3 racemic 2-azabicyclo[2.2.1]hept-5-en-3-one 
• 109000-07-9 2-(p-tolylsulfonyl)-2-azabicyclo<2.2.1>hept-5-en-3-one 

Downstream Products

• 118353-05-2 cis-<4-(hydroxymethyl)-2-cyclopentenyl>guanine 

Relevant articles and documents

Asymmetric synthesis of carbocyclic pyrimidine nucleosides via π-allylpalladium complex

Racemic and enantiomerically pure carbocyclic pyrimidine nucleosides were synthesized efficiently by a convergent approach using Trost nucleophilic addition of π-allylpalladium complexes.

Synthesis of carbocyclic nucleosides from 2-azabicyclo[2.2.1]hept-5-en-3-ones: Sodium borohydride-mediated carbon-nitrogen bond cleavage of five- and six-membered lactams

Various carbocyclic ribofuranosyl nucleosides were stereoselectively synthesized through a small number of steps from 2-azabicyclo[2.2.1]hept-5-en-3-ones by the use of sodium borohydride-mediated C-N bond cleavage as a key step. Ready availability of a no