27087-14-5

Basic information

• Product Name: Oxiranemethanol, phenylcarbamate
• Synonyms: (phenylcarbamoyloxy-methyl)-oxirane;glycidyl phenylcarbamate;Glycidyl-N-phenylcarbamat;Phenyl-carbamidsaeure-(2,3-epoxy-propylester);2,3-epoxipropyl-N-phenylcarbamate;phenyl-carbamic acid-(2,3-epoxy-propyl ester);Oxiranemethanol,phenylcarbamate
• CAS NO: 27087-14-5
• Molecular Formula: C10H11NO3
• Molecular Weight: 193.202
• Mol File: 27087-14-5.mol
• Article Data: 3

Chemical Properties

• Melting Point: 59.8-60.0 °C(Solv: ethyl ether (60-29-7); ligroine (8032-32-4))
• Boiling Point: 270.6±13.0 °C(Predicted)
• Density: 1.295±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Oxiranemethanol, phenylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: Oxiranemethanol, phenylcarbamate(27087-14-5)
• EPA Substance Registry System: Oxiranemethanol, phenylcarbamate(27087-14-5)

Safety Data

• Hazardous Substances Data: 27087-14-5(Hazardous Substances Data)

Upstream product

• 556-52-5 oxiranyl-methanol 
• 103-71-9 phenyl isocyanate 

Downstream Products

• 27087-15-6 3-phenyl-4-hydroxymethyl-2-oxo-1,3-oxazolidine 
• 99360-02-8 phenyl-carbamic acid-(3-chloro-2-hydroxy-propyl ester) 

Relevant articles and documents

Synthesis of multifunctional 4-hydroxymethyl 2-oxazolidinones from glycidyl carbamate derivatives catalyzed by bicyclic guanidine

4-Hydroxymethyl 2-oxazolidinones have been successfully synthesized under mild conditions by the intramolecular cyclization of glycidyl carbamate derivatives with a bicyclic guanidine as the efficient catalyst. This reaction system, which is also applicab

Irreversible inactivation of papain and cathepsin B by epoxidic substrate analogues

Epoxidic substrate analogues related to allylamine (4a-4e) and allyl alcohol (5a-5f) were synthesized and tested as models of cysteine-protease inhibitors.They proved to be irreversible inhibitors of papain and cathepsin B with pseudo-first-order inactiva