946392-52-5

Basic information

• Product Name: (1S)-1-[(1S,2S,4R)-2-(tert-butyldiphenylsilyloxy)-4-(hydroxymethyl)cyclobutyl]-1,2-ethanediol
• CAS NO: 946392-52-5
• Molecular Weight: 400.59
• Mol File: 946392-52-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1S)-1-[(1S,2S,4R)-2-(tert-butyldiphenylsilyloxy)-4-(hydroxymethyl)cyclobutyl]-1,2-ethanediol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S)-1-[(1S,2S,4R)-2-(tert-butyldiphenylsilyloxy)-4-(hydroxymethyl)cyclobutyl]-1,2-ethanediol(946392-52-5)
• EPA Substance Registry System: (1S)-1-[(1S,2S,4R)-2-(tert-butyldiphenylsilyloxy)-4-(hydroxymethyl)cyclobutyl]-1,2-ethanediol(946392-52-5)

Safety Data

• Hazardous Substances Data: 946392-52-5(Hazardous Substances Data)

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 139230-94-7 (-)-(S)-5-pivaloyloxymethyl-2(5H)-furanone 
• 946392-42-3 (1R,4S,5S)-4-pivaloyloxymethyl-3-oxabicyclo[3.2.0]heptane-2,6-dione 
• 946392-50-3 (1R,4S,5R,6S)-6-hydroxy-4-pivaloyloxymethyl-3-oxabicyclo[3.2.0]heptan-2-one 

Downstream Products

• 946392-54-7 (1R,2S,3S)-3-tert-butyldiphenylsilyloxy-2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]cyclobutane-1-carbaldehyde 
• 946392-55-8 {(1S,2S,3S)-3-tert-butyldiphenylsilyloxy-2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]cyclobutyl}methanol 
• 946392-56-9 {(1S,2S,3S)-3-(tert-butyldiphenylsilyloxy)-2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]cyclobutyl}methyl benzoate 
• 946392-44-5 {(1S,2R,3S)-2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-hydroxycyclobutyl}methyl benzoate 
• 946392-57-0 {(1S,2S,3S)-2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-(methylsulfonyloxy)cyclobutyl}methyl benzoate 
• 946392-58-1 9-{(1R,2R,3S)-3-benzoyloxymethyl-2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]cyclobut-1-yl}adenine 
• 946392-43-4 {(1R,2S,3S)-3-tert-butyldiphenylsilyloxy-2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]cyclobutyl}methanol 

Relevant articles and documents

Stereoselective route to oxetanocin carbocyclic analogues based on a [2 + 2] photocycloaddition to a chiral 2(5H)-furanone

The synthesis of the trisubstituted cyclobutane 7, which is a suitable precursor for the preparation of oxetanocin carbocyclic analogues, is described. The key step involves a regio- and diastereoselective [2 + 2] photochemical reaction of ketene diethyl