169872-81-5

Basic information

• Product Name: (1S,4R)-cis-1-phenoxy-2-cyclopentene-4-ol
• Synonyms: (1S,4R)-cis-1-phenoxy-2-cyclopentene-4-ol
• CAS NO: 169872-81-5
• Molecular Weight: 176.215
• Mol File: 169872-81-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1S,4R)-cis-1-phenoxy-2-cyclopentene-4-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,4R)-cis-1-phenoxy-2-cyclopentene-4-ol(169872-81-5)
• EPA Substance Registry System: (1S,4R)-cis-1-phenoxy-2-cyclopentene-4-ol(169872-81-5)

Safety Data

• Hazardous Substances Data: 169872-81-5(Hazardous Substances Data)

Upstream product

• 7129-41-1 6-oxabicyclo[3.1.0]hex-2-ene 
• 108-95-2 phenol 
• 128741-00-4 (1S,4R)-cis-1-ethoxycarbonyloxy-4-acetoxy-2-cyclopentene 
• 60410-16-4 (1R,4S)-4-hydroxy-2-cyclopentene-1-yl acetate 
• 54664-61-8 cis-1,4-diacetoxy-2-cyclopentene 
• 210701-09-0 1-acetoxy-4-phenoxy-2-cyclopentene 
• 108-22-5 Isopropenyl acetate 
• 103056-56-0 (+/-)-cis-4-phenyloxy-2-cyclopenten-1-ol 

Downstream Products

• 210701-06-7 1-Bromo-2-((1S,4S)-4-phenoxy-cyclopent-2-enyloxy)-benzene 
• 210701-08-9 (1S,4S)-trans-1-phenoxy-4-(2,4,6-tribromophenoxy)-2-cyclopentene 

Relevant articles and documents

Process for producing cycloalkyl [b]benzofurans

The present invention provides a process for producing an optically active compound of cycloalkyl[b]benzofuran using a readily available optically active compound as a starting material by a reaction using a transition metal or the Mitsunobu reaction, or

Chemoenzymatic synthesis of trans-4,5-dihydroxycyclopent-2-enones: Conversion to D-1-deoxynojirimycin

(4R,5S)-trans-4,5-Bis(tert-butyldimethylsilyloxy)cyclopent-2-enone 8 and (4R,5S)-trans-4,5-di(benzyloxy)cyclopent-2-enone 20 are prepared by equilibration of the corresponding cis derivatives; enone 8 is transformed into the glucosidase inhibitor, D-1-deoxynojirimycin 14.