107986-04-9

Basic information

• Product Name: ω-<(4-tert-Butylphenyl)hydrazono>-ω,2,4-trichloracetophenon
• CAS NO: 107986-04-9
• Molecular Weight: 383.705
• Mol File: 107986-04-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ω-<(4-tert-Butylphenyl)hydrazono>-ω,2,4-trichloracetophenon(CAS DataBase Reference)
• NIST Chemistry Reference: ω-<(4-tert-Butylphenyl)hydrazono>-ω,2,4-trichloracetophenon(107986-04-9)
• EPA Substance Registry System: ω-<(4-tert-Butylphenyl)hydrazono>-ω,2,4-trichloracetophenon(107986-04-9)

Safety Data

• Hazardous Substances Data: 107986-04-9(Hazardous Substances Data)

Upstream product

• 769-92-6 4-tert-Butylaniline 
• 4252-78-2 2,2',4'-trichloroacetophenone 

Downstream Products

• 107986-26-5 1-(4-tert-Butylphenyl)-3-(2,4-dichlorbenzoyl)-1H-<1,2,4>triazolo<3,4-c>-1,2,4-triazol 
• 107986-15-2 ω-(3-Amino-4H-1,2,4-triazol-4-yl)-2,4-dichlor-ω-<(4-tert-butylphenyl)hydrazono>-2,4-dichloracetophenon 

Relevant articles and documents

3-Aroyl-1-aryl-1H-triazolo-1,2,4-triazoles, Investigation of the Reaction Pathway by X-Ray Analysis and Molecular Modelling

ω-Halogen-ω-(phenylhydrazono)acetophenones (6a-l) with electron-withdrawing substituents in the acetophenone moiety react with 3-amino-4H-1,2,4-triazole (2) to form monocyclic substitution products, ω-(3-amino-1,2,4-triazol-4-yl)-ω-(phenylhydrazono)acetophenones (7a-l).The latter yield bicyclic 3-aroyl-1-aryl-1H-triazolo-1,2,4-triazoles (8a-l).With 5 amino-3-methyl-1H-pyrazole (14) or 5-aminotetrazole (19) instead of 2, the reaction takes another course in each case.The differing reaction pathways are discussed by means of X-ray analysis and molecular modelling.