321947-56-2

Upstream product

• 13222-85-0 p-methylbenzoic anhydride 
• 3096-70-6 3,5-dimethyl-4-aminophenol 

Downstream Products

• 873856-06-5 4-amino-3,5-dimethyl-2-chloro-N-(4-methylbenzoyl)phenol 
• 873856-11-2 4-amino-3,5-dimethyl-N-(4-methylbenzoyl)-2,6-dichlorophenol 
• 873856-14-5 3,5-dimethyl-N-(4-methylbenzoyl)-2,6-dichloro-1,4-benzoquinone monoimine 
• 893654-36-9 3,5-dimethyl-4-(4-methylbenzoyl)imino-2,5,6,6-tetrachlorocyclohex-2-en-1-one 
• 1239917-67-9 4-amino-2-bromo-3,5-dimethyl-N-(4-methylbenzoyl)phenol 
• 873856-22-5 4-amino-2,6-diromo-3,5-dimethyl-N-(4-methylbenzoyl)phenol 
• 873856-24-7 2,6-dibromo-3,5-dimethyl-N-(4-methylbenzoyl)-1,4-benzoquinone monoimine 
• 1239917-68-0 2,5,6,6-tetrabromo-3,5-dimethyl-4-(4-methylbenzoyl)iminocyclohex-2-en-1-one 
• 446269-13-2 N-(1-ethoxy-2,6-dimethyl-4-oxocyclohexa-2,5-dien-1-yl)-4-methylbenzamide 
• 446269-09-6 N-(1-methoxy-2,6-dimethyl-4-oxocyclohexa-2,5-dien-1-yl)-4-methylbenzamide 

Relevant academic research and scientific papers

Halogenation of N-substituted para-quinone monoimines and para-quinone monoximes ethers: IX. Halogenation of N-aroyl-2,6(3,5)-dimethyl-1,4-benzoquinone monoimines and their reduced forms

At the halogenation of N-aroyl-2,6(3,5)-dimethyl-1,4-benzoquinone imines we found the halogenation of methyl groups to occur. The bromination of N-aroyl-2,6-dimethyl-1,4-benzoquinone imines yielded 3,6-dibromo-2,6-dimethyl-5-aroyloxycyclohex-2-ene-1,4-dio