86072-19-7

Basic information

• Product Name: methyl N-cyclohexyloxamate
• Synonyms: methyl N-cyclohexyloxamate
• CAS NO: 86072-19-7
• Molecular Weight: 185.223
• Mol File: 86072-19-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: methyl N-cyclohexyloxamate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl N-cyclohexyloxamate(86072-19-7)
• EPA Substance Registry System: methyl N-cyclohexyloxamate(86072-19-7)

Safety Data

• Hazardous Substances Data: 86072-19-7(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 1132-42-9 N-cyclohexylacetoacetamide 
• 5781-53-3 monomethyl oxalyl chloride 
• 108-91-8 cyclohexylamine 
• 23144-68-5 trichloro-acetic acid cyclohexylamide 

Downstream Products

• 861012-03-5 N-cyclohexyl-N'-picryl-oxalamide 
• 51176-78-4 N-cyclohexyl-N'-(2,4-dinitro-phenyl)-oxalamide 
• 3173-53-3 Cyclohexyl isocyanate 
• 3299-64-7 N,N'-dicyclohexyloxamide 
• 1541-19-1 ethyl N-cyclohexylcarbamate 
• 13144-62-2 2-(cyclohexylamino)-2-oxoacetic acid 
• 873966-35-9 N-cyclohexyl-N'-o-tolyl-oxalamide 
• 702647-33-4 N-cyclohexyl-N'-m-tolyl-oxalamide 
• 861012-10-4 N-cyclohexyl-N'-(4-nitro-phenyl)-oxalamide 

Relevant articles and documents

Asymmetric Transfer Hydrogenation of α-Keto Amides; Highly Enantioselective Formation of Malic Acid Diamides and α-Hydroxyamides

The asymmetric transfer hydrogenation (ATH) of α-keto-1,4-diamides using a tethered Ru/TsDPEN catalyst was achieved in high ee. Studies on derivatives identified the structural elements which lead to the highest enantioselectivities in the products. The α-keto-amide reduction products have been converted to a range of synthetically valuable derivatives.

Oxamyl dipeptide caspase inhibitors developed for the treatment of stroke

Structural modifications were made to a previously described acyl dipeptide caspase inhibitor, leading to the oxamyl dipeptide series. Subsequent SAR studies directed toward the warhead, P2, and P4 regions of this novel peptidomimetic are described herein.

Reactivity of Carbamoyl Radicals. A New, General, Convenient Free-Radical Synthesis of Isocyanates from Monoamides of Oxalic Acid

A new, general, simple synthesis of isocyanates was developed by oxidation of monoamides of oxalix acid with peroxydisulfate catalyzed by Ag and Cu salts.The reaction was carried out in a two-phase system (water and an organic solvent), and it is suitable also for practical applications, due to the simple experimental conditions and the inexpensive as well as nontoxic reagents.The first example of homolytic intramolecular aromatic carbamoylation is also reported.