5070-30-4

Basic information

• Product Name: Butanamide, N-cyclohexyl-2-oxo-
• CAS NO: 5070-30-4
• Molecular Formula: C10H17NO2
• Molecular Weight: 183.25
• Mol File: 5070-30-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Butanamide, N-cyclohexyl-2-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: Butanamide, N-cyclohexyl-2-oxo-(5070-30-4)
• EPA Substance Registry System: Butanamide, N-cyclohexyl-2-oxo-(5070-30-4)

Safety Data

• Hazardous Substances Data: 5070-30-4(Hazardous Substances Data)

Upstream product

• 942020-76-0 N-cyclohexyl-2-ethylimidazo[1,2-a]pyridin-3-amine 
• 108-91-8 cyclohexylamine 
• 80465-30-1 N-carboxy 2-amino-2-butenoic acid anhydride 
• 931-53-3 Cyclohexyl isocyanide 
• 1487-67-8 N-(1-chloropropylidene)-N-methylmethanaminium chloride 

Downstream Products

• 13606-94-5 N-(pyridine-2-yl)propionamide 
• 108-91-8 cyclohexylamine 
• 2387-23-7 1,3-Dicyclohexylurea 

Relevant articles and documents

Diverse Oxidative C(sp2)-N Bond Cleavages of Aromatic Fused Imidazoles for Synthesis of α-Ketoamides and N-(pyridin-2-yl)arylamides

An efficient and chemoselective C(sp2)-N bond cleavage of aromatic imidazo[1,2-a]pyridine molecules is developed. A broad scope of amide compounds such as α-ketoamides and N-(pyridin-2-yl)arylamides are afforded as the final products in up to quantitative yields. Diverse C-N bond cleavages are controlled by the oxidative species used in this transformation, with various amide products afforded in a chemoselective fashion. A preliminary study indicated that some α-ketoamides exhibit anti-Tobacco Mosaic Virus activity for potential use in plant protection.

Dehydrooligopeptides. V. Synthesis of N-carboxy α-dehydroamino acid anhydrides and their transformation of α-dehydroamino acid and dehydrooligopeptide derivatives

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