37854-32-3

Basic information

• Product Name: 1,2-Cyclopentanediol, diacetate, cis-
• CAS NO: 37854-32-3
• Molecular Formula: C9H14O4
• Molecular Weight: 186.208
• Mol File: 37854-32-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-Cyclopentanediol, diacetate, cis-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Cyclopentanediol, diacetate, cis-(37854-32-3)
• EPA Substance Registry System: 1,2-Cyclopentanediol, diacetate, cis-(37854-32-3)

Safety Data

• Hazardous Substances Data: 37854-32-3(Hazardous Substances Data)

Upstream product

• 5057-99-8 trans-cyclopentane-1,2-diol 
• 108-24-7 acetic anhydride 

Downstream Products

• 930-46-1 (1R,2R)-cyclopentane-1,2-diol 
• 20520-67-6 (1R,2R)-2-hydroxycyclopentyl acetate 
• 63261-45-0 (S,S)-cyclopentane-1,2-diol 
• 20520-67-6 (S,S)-2-acetoxycyclopentan-1-ol 
• 133442-59-8 (R,R)-1,2-diacetoxycyclopentane 
• 105663-23-8 (S,S)-1,2-diacetoxycyclopentane 
• 542-92-7 cyclopenta-1,3-diene 
• 20520-67-6 (+/-)-cis-1-acetoxy-2-hydroxycyclopentane 
• 241147-40-0 (1R,2R)-2-Methoxymethoxy-cyclopentanol 
• 864658-75-3 (1S,2R)-2-Methoxymethoxy-cyclopentanol 
• 864658-67-3 (1R,2S)-2-((R)-2-Benzyloxy-dodec-4-ynyloxy)-cyclopentanol 
• 864658-76-4 [(R)-1-((1S,2R)-2-Methoxymethoxy-cyclopentyloxymethyl)-undec-3-ynyloxymethyl]-benzene 
• 864658-68-4 (R)-2-[(1R,2S)-2-((R)-2-Benzyloxy-dodec-4-ynyloxy)-cyclopentyloxymethyl]-oxirane 
• 864658-69-5 (R)-1-[(1R,2S)-2-((R)-2-Benzyloxy-dodec-4-ynyloxy)-cyclopentyloxy]-5-trimethylsilanyl-pent-4-yn-2-ol 

Relevant articles and documents

Synthesis of non-THF analogs of acetogenin toward simplified mimics

Acetogenin analogs in which the bis-adjacent THF ring was replaced with an enantioselectively synthesized 1,2-cyclopentanediol bis-ether skeleton were synthesized to obtain simplified mimics, and their inhibitory effect on mitochondrial NADH-ubiquinone oxidoreductase (complex I) was examined. The results clearly demonstrate that the 1,2-cyclopentanediol bis-ether motif can substitute for the bis-THF ring while maintaining very potent inhibitory activity at the nanomolar level.

Direct one step mono-functionalisation of symmetrical 1,2-diols

The mono-functionalisation of meso- and C2-symmetric diols has been achieved via the use of a new lanthanide(III) chloride catalysed acylation reaction. (C) 2000 Elsevier Science Ltd.