70584-30-4

Basic information

• Product Name: N-cyclohexyl-3,5-dimethyl-1H-pyrazole-1-carboxamide
• Synonyms: N-cyclohexyl-3,5-dimethyl-1H-pyrazole-1-carboxamide
• CAS NO: 70584-30-4
• Molecular Weight: 221.302
• Mol File: 70584-30-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-cyclohexyl-3,5-dimethyl-1H-pyrazole-1-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-cyclohexyl-3,5-dimethyl-1H-pyrazole-1-carboxamide(70584-30-4)
• EPA Substance Registry System: N-cyclohexyl-3,5-dimethyl-1H-pyrazole-1-carboxamide(70584-30-4)

Safety Data

• Hazardous Substances Data: 70584-30-4(Hazardous Substances Data)

Upstream product

• 67-51-6 3,5-dimethyl-1H-pyrazole 
• 3173-53-3 Cyclohexyl isocyanate 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 108-91-8 cyclohexylamine 
• 129370-61-2 {copper(I)(3,5-dimethyl-pz-C(O)-NC₆H₁₁)(cyclohexyl isocyanide)} 
• 123-54-6 acetylacetone 
• 52662-76-7 (N-cyclohexylhydrazinecarboxamide) 

Downstream Products

• 10354-42-4 N-cyclohexylthiophene-2-carboxamide 
• 7474-36-4 N-cyclohexylcyclohexanecarboxamide 
• 41846-01-9 N-cyclohexylheptanamide 
• 17427-96-2 N-cyclohexyl-palmitoyl amide 

Relevant articles and documents

Rhodium(III)-catalyzed Intermolecular Unactivated Secondary C(sp3)?H Bond Amidation Directed by 3,5-dimethylpyrazole

A Rh(III)-catalyzed intermolecular unactivated secondary C(sp3)?H bond amidation via nitrene insertion directed by 3,5-dimethylpyrazole is reported. This procedure tolerates a broad substrate scope including chain and cyclic N-alklyamides. Notably, the directing group 3,5-dimethylpyrazole of chain N-alkylamide substrates could be easily removed via cascade intermolecular amidation and intramolecular cyclization in one-pot affording the sulfonylureas by increasing the reaction temperature. (Figure presented.).