144938-82-9

Basic information

• Product Name: 2-Cyclopentene-1-methanol, 4-hydroxy-, (1R,4S)-
• CAS NO: 144938-82-9
• Molecular Formula: C6H10O2
• Molecular Weight: 114.144
• Mol File: 144938-82-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-Cyclopentene-1-methanol, 4-hydroxy-, (1R,4S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclopentene-1-methanol, 4-hydroxy-, (1R,4S)-(144938-82-9)
• EPA Substance Registry System: 2-Cyclopentene-1-methanol, 4-hydroxy-, (1R,4S)-(144938-82-9)

Safety Data

• Hazardous Substances Data: 144938-82-9(Hazardous Substances Data)

Upstream product

• 25125-21-7 4-(hydroxymethyl)cyclopentene 

Downstream Products

• 144938-80-7 (1S,2R,3S,4S)-(-)-4-(Hydroxymethyl)cyclopentane-1,2,3-triol 
• 261511-29-9 (3aR,4R,6R,6aS)-4-Benzyloxymethyl-6-iodohexahydrocyclopenta[b]furan-2-one 
• 261511-37-9 (1R,4R,5S)-(5-Benzyloxymethyl-4-methylcyclopent-2-en-1-yl)acetic acid 
• 485-43-8 iridomyrmecin 
• 261511-24-4 [(1S)-cis-1-(4-Benzyloxymethylcyclopent-2-en-1-yloxy)ethenyloxy] tert-butyldimethylsilane 
• 193141-50-3 (3aR,4R,6aS)-4-Benzyloxymethyl-3,3a,4,6a-tetrahydrocyclopenta[b]furan-2-one 
• 193071-32-8 (1S)-cis-(5-Benzyloxymethylcyclopent-2-en-1-yl)acetic acid 
• 193071-31-7 (1S)-cis-4-Benzyloxymethylcyclopent-2-en-1-yl acetate 
• 261511-35-7 (2S)-[(1S,4S,5R)-4-Benzyloxymethyl-4-methylcyclopent-2-en-1-yl]propanoic acid 
• 261511-33-5 (3S,3aS,4R,6aS)-4-Benzyloxymethyl-3,3a,4,6a-tetrahydro-3-methylcyclopenta[b]furan-2-one 
• 371783-77-6 (1'R,4'R)-tert-butyldimethyl-(4-phenylsulfanylcyclopent-2-enylmethoxy)-silane 
• 371783-79-8 (1''RS,1'R,4'R)-[4-(2-bromo-1-ethoxy-ethoxymethyl)cyclopent-2-enyllsulfanyl]-benzene 
• 371783-78-7 (1'R,4'R)-(+)-(4-phenylsulfanyl-cyclopent-2-enyl)methanol 
• 261511-22-2 (1S)-cis-4-Benzyloxymethylcyclopent-2-en-1-ol 

Relevant articles and documents

Highly Enentioselective Rearrangement of a meso-Epoxide to an Allyl Alcohol for Carbocyclic Nucleoside Synthesis: an Internal Alkoxide Effect

The synthesis of enantiomeric cis-4-(hydroxymethyl)cyclopent-2-ene-1-ols 2 and 3 (R=H) via a highly enantioselective rearrangement of cis-6-oxabicyclohexane-3-methanol 4 (R=H) using the dilithium salts of (+)- or (-)-norephedrine is described.