85029-84-1

Basic information

• Product Name: dihydro-6'-hydroxyspiro[cyclohexane-1,2'-furo[3,4-d][1,3]dioxol]-4'(3'aH)-one
• Synonyms: dihydro-6'-hydroxyspiro[cyclohexane-1,2'-furo[3,4-d][1,3]dioxol]-4'(3'aH)-one;6,6a-Dihydro-6-hydroxyspiro[furo[3,4-d][1,3]dioxole-2,1'-cyclohexan]-4(3aH)-one;Einecs 285-109-3
• CAS NO: 85029-84-1
• Molecular Formula: C₁₀H₁₄O₅
• Molecular Weight: 212.19928
• EINECS: 285-109-3
• Mol File: 85029-84-1.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: dihydro-6'-hydroxyspiro[cyclohexane-1,2'-furo[3,4-d][1,3]dioxol]-4'(3'aH)-one(CAS DataBase Reference)
• NIST Chemistry Reference: dihydro-6'-hydroxyspiro[cyclohexane-1,2'-furo[3,4-d][1,3]dioxol]-4'(3'aH)-one(85029-84-1)
• EPA Substance Registry System: dihydro-6'-hydroxyspiro[cyclohexane-1,2'-furo[3,4-d][1,3]dioxol]-4'(3'aH)-one(85029-84-1)

Safety Data

• Hazardous Substances Data: 85029-84-1(Hazardous Substances Data)

Upstream product

• 40656-50-6 2,3:5,6-di-O-cyclohexylidene-D-gulonic acid γ-lactone 
• 108-94-1 cyclohexanone 
• 111005-66-4 2,3-O-cyclohexylidene-D-gulonic acid γ-lactone 

Relevant articles and documents

Enantiospecific Syntheses of Aristeromycin and Neplanocin A

The carbocylic nucleosides (-)-aristeromycin and (-)-neplanocin A were made enantiospecifically in nine steps and ten steps, respectively, from D-ribonic acid γ-lactone.Quenching of an organocuprate conjugate addition reaction with either acetic acid or methanesulfinyl chloride determines whether the divergent synthetic route branches toward (-)-aristeromycin or (-)-neplanocin A.An alternate synthesis of cyclopentenone 1, a common intermediate to these compounds, from D-gulonic acid γ-lactone is also described.