144874-54-4

Basic information

• Product Name: (1R,2R,3R,5S)-(-)-3-Acetoxy-5-(triphenylmethoxymethyl)cyclopentane-1,2-diol
• CAS NO: 144874-54-4
• Molecular Weight: 432.516
• Mol File: 144874-54-4.mol

Chemical Properties

• CAS DataBase Reference: (1R,2R,3R,5S)-(-)-3-Acetoxy-5-(triphenylmethoxymethyl)cyclopentane-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R,3R,5S)-(-)-3-Acetoxy-5-(triphenylmethoxymethyl)cyclopentane-1,2-diol(144874-54-4)
• EPA Substance Registry System: (1R,2R,3R,5S)-(-)-3-Acetoxy-5-(triphenylmethoxymethyl)cyclopentane-1,2-diol(144874-54-4)

Safety Data

• Hazardous Substances Data: 144874-54-4(Hazardous Substances Data)

Upstream product

• 137760-86-2 (+/-)-3β-Acetoxy-5β-(triphenylmethoxymethyl)cyclopentene 
• 110289-12-8 (+/-)-(1β,4β)-1-(triphenylmethoxymethyl)cyclopent-2-en-4-ol 
• 144938-69-2 (-)-(3R,5S)-3-Acetoxy-5-(triphenylmethoxymethyl)cyclopentene 
• 137821-21-7 (1S,4R)-(-)-1-(triphenylmethoxymethyl)cyclopent-2-en-4-ol 

Downstream Products

• 144874-55-5 (+/-)-2α,3α-Isopropylidenedioxy-4β-(triphenylmethoxymethyl)cyclopentane-1β-ol 
• 144874-55-5 (+/-)-2α,3α-Isopropylidenedioxy-4β-(triphenylmethoxymethyl)cyclopentan-1α-ol 
• 129885-83-2 (+/-)-2α,3α-Isopropylidenedioxy-4β-(triphenylmethoxymethyl)cyclopentanone 
• 129885-83-2 (3aR,6R,6aR)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-cyclopenta[1,3]dioxol-4-one 
• 113299-31-3 (1S,2S,3R,4R)-(+)-4-(Hydroxymethyl)cyclopentane-1,2,3-triol 
• 144938-78-3 (1S,2S,3R,4R)-(-)-2,3-Isopropylidenedioxy-4-(triphenylmethoxymethyl)cyclopentanol 
• 144938-75-0 (1R,2S,3R,4R)-(-)-2,3-Isopropylidenedioxy-4-(triphenylmethoxymethyl)cyclopentanol 
• 144874-56-6 (1R,2S,3R,4R)-(-)-1-Acetoxy-2,3-(isopropylidenedioxy)-4-(triphenylmethoxymethyl)cyclopentane 
• 144874-56-6 (+/-)-1β-Acetoxy-2α,3α-(isopropylidenedioxy)-4β-(triphenylmethoxymethyl)cyclopentane 

Relevant articles and documents

Synthesis of pseudo-Ribofuranoses by Stereocontrolled Reactions on 4-Hydroxycyclopent-2-enylmethanol Derivatives

The diol 3 is a major product formed from a Prins reaction on cyclopentadiene and was readily converted into the derivatives 4-7.The latter compounds were obtained in states of high optical purity by using both enzyme-catalysed hydrolysis and esterificati