131184-65-1

Basic information

• Product Name: 4,4-ethylenedioxy-1-(phenoxycarbonyl)piperidine
• Synonyms: 4,4-ethylenedioxy-1-(phenoxycarbonyl)piperidine
• CAS NO: 131184-65-1
• Molecular Weight: 263.293
• Mol File: 131184-65-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4,4-ethylenedioxy-1-(phenoxycarbonyl)piperidine(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4-ethylenedioxy-1-(phenoxycarbonyl)piperidine(131184-65-1)
• EPA Substance Registry System: 4,4-ethylenedioxy-1-(phenoxycarbonyl)piperidine(131184-65-1)

Safety Data

• Hazardous Substances Data: 131184-65-1(Hazardous Substances Data)

Upstream product

• 177-11-7 4,4-ethylenedioxy-piperidine 
• 1885-14-9 phenyl chloroformate 
• 3612-20-2 1-phenylmethyl-4-piperidone 
• 108-95-2 phenol 
• 41979-37-7 4-oxo-piperidine-1-carboxylic acid phenyl ester 
• 107-21-1 ethylene glycol 

Downstream Products

• 41979-37-7 4-oxo-piperidine-1-carboxylic acid phenyl ester 
• 131184-64-0 1-<1-(2-benzodioxanylmethyl)-4-piperidyl>amino-3-(1-naphthoxy)-2-propanol 
• 177-11-7 4,4-ethylenedioxy-piperidine 

Relevant articles and documents

THIENOPYRIMIDINE AS CDC7 KINASE INHIBITORS

The present invention relates to a compound represented by the formula (I): wherein each symbol is as defined in the specification, or a salt thereof, or a prodrug thereof, which is useful for the prophylaxis or treatment of cancer

Carbamoylimidazolium salts as diversification reagents: An application to the synthesis of tertiary amides from carboxylic acids

An efficient method for the preparation of tertiary amides from carbamoylimidazolium salts and carboxylic acids is described. The transformation occurs at room temperature and under relatively mild conditions. The carbamoylimidazolium salts are obtained from the reaction of secondary amines with N,N′-carbonyldiimidazole, followed by methylation with methyl iodide. The utility of this reaction was demonstrated in the formation of Weinreb amides and in a short synthesis of fused bicyclic amides. The introduction of this reaction now permits carbamoylimidazolium salts to be utilized in the formation of tertiary amides, ureas, carbamates and thiocarbamates under a single set of conditions.