142095-47-4

Basic information

• Product Name: (+/-)-(1α,2β,4α)-4-benzamidocyclopentane-1,2-diol
• Synonyms: (+/-)-(1α,2β,4α)-4-benzamidocyclopentane-1,2-diol
• CAS NO: 142095-47-4
• Molecular Weight: 221.256
• Mol File: 142095-47-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (+/-)-(1α,2β,4α)-4-benzamidocyclopentane-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-(1α,2β,4α)-4-benzamidocyclopentane-1,2-diol(142095-47-4)
• EPA Substance Registry System: (+/-)-(1α,2β,4α)-4-benzamidocyclopentane-1,2-diol(142095-47-4)

Safety Data

• Hazardous Substances Data: 142095-47-4(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 142095-48-5 trans-3-dibenzamido-6-oxabicyclo<3.1.0>hexane 
• 142095-45-2 (cyclopent-3-en-1-yl)dibenzamide 
• 132065-12-4 4-benzamidocyclopentene 
• 27721-59-1 (3-cyclopenten-1-yl)amine 
• 142095-49-6 (+/-)-trans-4-benzamido-3-cyano-3-phenyl-7-trimethylsilyloxy-2-oxa-4-azabicyclo<3.2.1>octane 
• 132065-13-5 cis-4-benzoylaminocyclopentene oxide 

Downstream Products

• 132065-10-2 (+/-)-(1α,2β,4β)-4-(6-amino-9H-purin-9-yl)-1,2-cyclopentanediol 
• 140438-62-6 (+/-)-2-amino-1,9-dihydro-9-<(1'α,3'β,4'β)-(3',4'dihydroxy-1'cyclopentyl)>-6H-purin-6-one 
• 140438-63-7 (+/-)-(1α,2β,4β)-4-(2,6-diamino-9H-purin-9-yl)-1,2-cyclopentanediol 
• 140438-65-9 (+/-)-(1α,2β,4β)-4-<<2-amino-6-chloro-5<(4-chlorophenyl)-azo>pyrimidin-4-yl>amino>-1,2-cyclopentanediol 
• 132065-14-6 (+/-)-(1α,3α,4β)-N-<3,4-bis(acetyloxy)cyclopentenyl>benzamide 

Relevant articles and documents

The synthesis of two 2'-deoxy carbocyclic purine nucleosides lacking the 5'-methylene

The synthesis of the adenine derivative (±)-(1α,2β,4α)-4-(6-amino-9H-purin-9-yl)-1,2-cyclopentanediol (2) and its hypoxanthine analogue (3) as carbocyclic nucleosides lacking the 5'-methylene is described in 7 steps from 3-cyclopenten-1-ylamine hydrochlor

Synthesis of 2-oxa-4-azabicyclo[3.2.1]-octane and -octene systems via X-ray-analyzed trans-3-dibenzamido-cyclopentene-1-oxide

3,4-trans-Epoxidation of (cyclopent-3-en-1-yl)dibenzamide gave, in 82% yield, the 1,5-epoxide, the structure of which was confirmed by X-ray crystallographic analysis. Epoxide ring opening by trimethylsilyl cyanide, under the catalysis of diethylaluminum