58936-18-8

Basic information

• Product Name: Carbonic acid benzyl ester 3,5-dioxo-10-oxa-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-4-yl ester
• Synonyms: Carbonic acid benzyl ester 3,5-dioxo-10-oxa-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-4-yl ester
• CAS NO: 58936-18-8
• Molecular Weight: 315.282
• Mol File: 58936-18-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Carbonic acid benzyl ester 3,5-dioxo-10-oxa-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-4-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbonic acid benzyl ester 3,5-dioxo-10-oxa-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-4-yl ester(58936-18-8)
• EPA Substance Registry System: Carbonic acid benzyl ester 3,5-dioxo-10-oxa-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-4-yl ester(58936-18-8)

Safety Data

• Hazardous Substances Data: 58936-18-8(Hazardous Substances Data)

Upstream product

• 501-53-1 benzyl chloroformate 
• 5596-17-8 exo‐N‐hydroxy‐7‐oxabicyclo[2.2.1]hept‐5‐ene‐2,3‐dicarboximide 

Downstream Products

• 58936-19-9 benzyl N-maleimidyl carbonate 

Relevant articles and documents

Synthesis of N-Hydroxymaleimide and N-Hydroxyitaconimide and their Related Derivatives

Thermolysis of alkyl and aryl carbonates of N-hydroxy-3,6-epoxy-1,2,3,6-tetrahydrophthalimide yielded the corresponding alkyl or aryl N-maleimidyl carbonates.The benzyl or phenyl carbonate afforded N-hydroxymaleimide, either by treatment with trifluoroacetic acid or by refluxing in methanol.N-hydroxyitaconimide was obtained by dehydration of N-hydroxyitaconamic acid with dicyclohexylcarbodi-imide (DCC).The DCC dehydration of N-acetoxy- and N-benzyloxy-itaconamic acids produced iminofuranones, which could be rearranged to imides.Deacylation of N-acetoxymaleimide was unsuccessful, whereas aminolysis of N-acetoxyitaconimide yielded the N-hydroxyimide.