461672-49-1

Upstream product

• 1128-28-5 4-aminothymol 
• 4513-25-1 N-phenylsulfonylbenzimidoyl chloride 
• 461672-43-5 N-[4-hydroxy-2-methyl-5-(propan-2-yl)phenyl]-N'-(phenylsulfonyl)benzimidamide 

Downstream Products

• 1332847-31-0 N-(3-chloro-4-hydroxy-5-isopropyl-2-methylphenyl)-N'-(phenylsulfonyl)benzenecarboximidamide 
• 1332847-48-9 N-(3-chloro-5-isopropyl-2-methyl-4-oxocyclohexa-2,5-dien-1-ylidene)-N'-(phenylsulfonyl)benzenecarboximidamide 
• 1332847-65-0 N-(3-bromo-4-hydroxy-5-isopropyl-2-methylphenyl)-N'-(phenylsulfonyl)benzenecarboximidamide 
• 1393690-02-2 N-[5,6-dichloro-6-methyl-4-oxo-3-(propan-2-yl)-cyclohex-2-en-1-ylidene]-N'-(phenylsulfonyl)benzimidamide 
• 1393690-18-0 N-[2,5-dibromo-4-hydroxy-6-methyl-3-(propan-2-yl)phenyl]-N'-(phenylsulfonyl)benzimidamide 
• 1393690-24-8 N-[2,5-dibromo-6-methyl-4-oxo-3-(propan-2-yl)cyclohexa-2,5-dien-1-ylidene]-N'-(phenylsulfonyl)benzimidamide 
• 1332847-78-5 N-(3-bromo-5-isopropyl-2-methyl-4-oxocyclohexa-2,5-dien-1-ylidene)-N'-(phenylsulfonyl)benzenecarboximidamide 

Relevant academic research and scientific papers

Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime ethers: XIV.* halogenation of N-[arylsulfonylimino(phenyl)methyl]-2,5- dialkyl-1,4-benzoquinone monoimines and their reduction products

Despite steric hindrances created by the bulky substituent on the nitrogen atom, halogenation of 2,5-dialkyl-N-[arylsulfonylimino(phenyl)methyl]-1,4- benzoquinone monoimines fairly readily gives their derivatives having two halogen atoms in the quinoid ring. Pleiades Publishing, Ltd., 2012.

Hydrohalogenation of N-[arylsulfonylimino(phenyl)methyl]-1,4-benzoquinone monoimines having alkyl substituents in the quinoid ring

Hydrohalogenation of N-[arylsulfonylimino(phenyl)methyl]-2,5(3,5)-dimethyl- 1,4-benzoquinone monoimines follows exclusively the 1,4-addition pattern, whereas N-[arylsulfonylimino(phenyl)methyl]-2,6-dimethyl-1,4-benzoquinone monoimines take up hydrogen halides according to the 6,3-addition scheme.