5259-69-8

Usage

Type of compound

Cyclic compound

Functional groups

Hydroxyamino group and carbonitrile group

Usage

Organic synthesis and pharmaceutical research

Potential applications

Synthesis of other chemical compounds

Safety precautions

Handle with care, store and use according to proper safety guidelines

Hazardous properties

May have hazardous properties (specific hazards not provided in the material)

Upstream product

• 100-64-1 cyclohexanone-oxime 
• 143-33-9 sodium cyanide 
• 108-94-1 cyclohexanone 
• 62281-25-8 C₁₀H₂₀N₂OSi 
• 57910-94-8 1-(1-cyano-cyclohexyl)-1-hydroxy-3-phenyl-urea 
• 75-64-9 tert-butylamine 
• 16499-30-2 1-(dimethylamino)cyclohexanecarbonitrile 

Downstream Products

• 16603-34-2 1-cyano-1-nitrosocyclohexane 
• 66285-88-9 3-(4-chloro-phenyl)-1-(1-cyano-cyclohexyl)-1-hydroxy-urea 
• 57910-94-8 1-(1-cyano-cyclohexyl)-1-hydroxy-3-phenyl-urea 
• 66285-90-3 C₁₄H₂₃N₃O₂ 
• 66285-91-4 C₁₂H₂₁N₃O₂ 
• 13181-75-4 O-(2,4-dinitrophenyl) cyclohexanone oxime 
• 77329-08-9 1-(1-Cyanocyclohexyl)-1-hydroxy-2-(2,2,2-trichloroethyl)isourea 
• 100051-19-2 1-tetrahydro[1,2]oxazin-2-yl-cyclohexanecarbonitrile 
• 61029-83-2 1-(3,6-dihydro-[1,2]oxazin-2-yl)-cyclohexanecarbonitrile 
• 103502-29-0 1-(5-chloro-3,6-dihydro-[1,2]oxazin-2-yl)-cyclohexanecarbonitrile 
• 66286-12-2 C₂₁H₂₁ClN₄O₃ 
• 66286-09-7 4-imino-2-phenylimino-3-oxa-1-aza-spiro[4.5]decan-1-ol 
• 66286-10-0 2-(4-chloro-phenylimino)-4-imino-3-oxa-1-aza-spiro[4.5]decan-1-ol 
• 66286-08-6 1-(4-chloro-phenylcarbamoyloxy)-N²-phenyl-3-oxa-1-aza-spiro[4.5]decane-2,4-diylidenediamine 

Relevant academic research and scientific papers

New NO donors with antithrombotic and vasodilating activities, part 28: N-(1-cyanoalkyl)-N-hydroxyureas

Nineteen N-(1-cyanoalkyl)-N-hydroxyureas comprising aliphatic (3a-i, 4a, b, and 5a) and aromatic (3j-n, 4c, 5b) compounds were prepared, fourteen of them for the first time, and tested for antithrombotic (p.o. administration to rats, 60 mg/kg) effects. Th

Iminyl, Amidyl, and Carbamyl Radicals from O-Benzoyl Oximes and O-Benzoyl Hydroxamic Acid Derivatives.

Oxime benzoates and O-benzoyl hydroxamic acid derivatives react with tributylstannane in the presence of AIBN to give iminyl, amidyl, and carbamyl radicals which can be captured by an internal olefin.

Amidyl and Carbamyl Radicals by Stannane Mediated Cleavage of O-Benzoyl Hydroxamic Acid Derivatives.

O-Benzoyl hydroxamic acids react with tributylstannane in the presence of AIBN to give amidyl or carbamyl radicals which can be captured by an internal olefin.