153255-65-3

Upstream product

• 52744-72-6 (2-aminophenyl)diphenylmethanol 
• 79-11-8 chloroacetic acid 

Downstream Products

• 1380598-63-9 1,3,6-tribromo-9-phenylacridine 
• 1367685-23-1 2-butylsulfanylmethyl-4,4-diphenyl-4H-3,1-benzoxazine 
• 1367685-25-3 2-diethylaminomethyl-4,4-diphenyl-4H-3,1-benzoxazine 
• 339223-48-2 C₂₆H₂₆N₂O 
• 1367685-31-1 4,4-diphenyl-2-(phenylaminomethyl)-4H-3,1-benzoxazine 
• 1367685-33-3 C₂₈H₂₄N₂O 
• 1380598-57-1 1-[(imidazo[1,2-a]pyridin-2-ylamino)phenyl]diphenylmethanol 

Relevant academic research and scientific papers

RESEARCH ON 4H-3,1-BENZOXAZINES. 10. REACTIONS OF O-AMINOPHENYLDIPHENYLCARBINOL WITH HALOALKANOIC ACIDS

The conditions used to carry out the reaction of o-aminophenyldiphenylcarbinol with haloalkanoic acids and the structures of the resulting products are determined by the nature of the starting acid.

Studies of benzoxazines 16*. synthesis and reactivity of 2,4-substituted 4H-3,1-benzoxazines

A novel method has been developed for preparation of substituted 4H-3,1-benzoxazines via formation of tetrafluoroborates. The substitution of halogen in 2-(α-haloalkyl)-4,4-diphenyl-4H-3,1-benzoxazines by NH and SH nucleophiles was performed. The effect of electrophilic substitution in the annelated aromatic ring in a series of 2,4-substituted 4H-3,1-benzoxazines has been studied.