37892-73-2

Basic information

• Product Name: (1S,2S)-2-(4-Methoxy-phenyl)-cyclopentanol
• CAS NO: 37892-73-2
• Molecular Weight: 192.258
• Mol File: 37892-73-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1S,2S)-2-(4-Methoxy-phenyl)-cyclopentanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S)-2-(4-Methoxy-phenyl)-cyclopentanol(37892-73-2)
• EPA Substance Registry System: (1S,2S)-2-(4-Methoxy-phenyl)-cyclopentanol(37892-73-2)

Safety Data

• Hazardous Substances Data: 37892-73-2(Hazardous Substances Data)

Upstream product

• 104-01-8 4-Methoxyphenylacetic acid 
• 51230-91-2 2-(4-methoxyphenyl)-4-pentenoic acid 
• 19980-43-9 1-(trimethylsilyloxy)cyclopentene 
• 67-56-1 methanol 
• 122345-97-5 (S)-4-((1S,2R)-2-Hydroxy-cyclopentyl)-cyclohex-2-enone 
• 37892-73-2 trans-(CH₃OC₆H₄)(C₅H₈OH) 

Downstream Products

• 37892-73-2 (-)-trans-2-(p-Methoxyphenyl)-cyclopentanol 
• 24587-56-2 (-)-trans-2-(p-Methoxyphenyl)cyclopentyltosylat 
• 34665-81-1 5-hydroxy-5-(4-methoxyphenyl)valeric acid δ lactone 
• 61349-69-7 (±)-2-(4-methoxyphenyl)cyclopentan-1-one 
• 38805-87-7 (+/-)-trans-2-(p-Methoxyphenyl)cyclopentyl-phthalat 

Relevant articles and documents

Dual Activation of Unsaturated Amides with Schwartz's Reagent: A Diastereoselective Access to Cyclopentanols and N,O-Dimethylcyclopentylhydroxylamines.

The diastereoselective access to cyclopentanols and N,O-dimethylcyclopentylhydroxylamines from 4-pentenoic acid-derived Weinreb amides is described. Based on the concomitant generation of both the nucleophilic and the electrophilic poles by hydrozirconati