122081-17-8

Basic information

• Product Name: HONC(CH₃)C(CH₃)NNHC(O)C₆H₄CH₃-p
• Synonyms: HONC(CH₃)C(CH₃)NNHC(O)C₆H₄CH₃-p
• CAS NO: 122081-17-8
• Molecular Weight: 233.27
• Mol File: 122081-17-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: HONC(CH₃)C(CH₃)NNHC(O)C₆H₄CH₃-p(CAS DataBase Reference)
• NIST Chemistry Reference: HONC(CH₃)C(CH₃)NNHC(O)C₆H₄CH₃-p(122081-17-8)
• EPA Substance Registry System: HONC(CH₃)C(CH₃)NNHC(O)C₆H₄CH₃-p(122081-17-8)

Safety Data

• Hazardous Substances Data: 122081-17-8(Hazardous Substances Data)

Upstream product

• 135636-66-7 butane-2,3-dione mono-oxime 
• 3619-22-5 p-toluic hydrazide 

Downstream Products

• 122081-25-8 C₂₀H₂₁N₃O₃ 
• 121859-98-1 C₁₂H₁₃NO₃ 
• 122081-29-2 N-(4-methyl)benzoyl glycine ethylester 
• 122081-21-4 4-Methyl-benzoic acid 4,5-dimethyl-[1,2,3]triazol-1-yl ester 
• 99-94-5 p-Toluic acid 

Relevant articles and documents

Synthesis, structure, and acylating properties of 1-aroyloxy-4,5-dimethyl- 1,2,3-triazoles

Lead tetra-acetate oxidation of α-hydroxyimino aroylhydrazones of biacetyl (1) gives 1-aroyloxy-4,5-dimethyl-1,2,3-triazoles (2), the structures of which were confirmed by X-ray analysis. A mechanism for this reaction is discussed. The products (2) are effective aroylating agents for the amino function under mild conditions.