27383-59-1

Basic information

• Product Name: ethyl (2-hydroxyphenylcarbamoyl)formate
• Synonyms: ethyl (2-hydroxyphenylcarbamoyl)formate
• CAS NO: 27383-59-1
• Molecular Weight: 209.202
• Mol File: 27383-59-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: ethyl (2-hydroxyphenylcarbamoyl)formate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (2-hydroxyphenylcarbamoyl)formate(27383-59-1)
• EPA Substance Registry System: ethyl (2-hydroxyphenylcarbamoyl)formate(27383-59-1)

Safety Data

• Hazardous Substances Data: 27383-59-1(Hazardous Substances Data)

Upstream product

• 4755-77-5 Ethyl oxalyl chloride 
• 95-55-6 2-amino-phenol 
• 79-37-8 oxalyl dichloride 
• 824-38-4 potassium 2-nitrophenoxide 
• 17318-84-2 Ethyl o-Nitrophenyl Oxalate 

Downstream Products

• 3597-63-5 <1,4>-benzoxazine-2,3-dione 
• 1331746-16-7 C₁₁H₁₅N₃O₃ 
• 226215-85-6 (5R,4S,2R,16R)-N,N'-ethylene(4-methyl-5-phenyl-18,23-phenylene)-2,16-bisoxazolidine 
• 226215-83-4 N-(2'-hydroxyphenyl)-N'-<9S,10R-(10-hydroxy-9-methyl-10-phenyl)ethyl>ethylenediamine 
• 226215-82-3 N-(2'-hydroxyphenyl)-N'-<9S,10R-(10-hydroxy-9-methyl-10-phenyl)ethyl>oxamide 
• 203736-27-0 (1S,2R)-(-)-[N-(2-hydroxy-1-methyl-2-phenyl-ethyl)-N'-(2-hydroxy-phenyl)]oxalamide 

Relevant articles and documents

Triphenylphosphine-mediated synthesis of the E/Z isomers of methyl 6-(1,2-di(methoxycarbonyl))-8-(ethyl carbamoylformyl)-2-oxo-2H-chromene-4- carboxylate

Triphenylphosphine-mediated reaction of dimethyl acetylenedicarboxylate with ethyl (2-hydroxyphenylcarbamoyl)formate in boiling toluene produces a mixture of methyl 8-(ethyl carbamylformyl)-2-oxo-2H-chromene-4-carboxylate and the E/Z isomers of methyl 6-(

A Bis-Polydentate Oxamate-Based Achiral Ligand That Can Stabilize a Macrocyclic Mixed Valence Compound or Induce a 1D Helical Chain

The reaction of the N-(2-hydroxyphenyl)oxamate ligand (ohpma) has been investigated with cobalt(II) and copper(II) ions. It has led to two coordination compounds, (TMA)3[{CoIII(ohpma)2CoII(MeOH)2}sub

A new method for the preparation of unsymmetrical 1,4-substituted piperazine derivatives

Symmetrical and unsymmetrical N,N'-piperazine derivatives of (-)- norephedrine and o-aminophenol were synthesized stereoselectively in yields >70% by reduction of the corresponding N,N'-ethylenebisoxazolidine heterocycles. The stereochemistry at the ring fusion carbons was established by NMR spectroscopy and X-ray crystallography.