100514-27-0

Upstream product

• 99-55-8 2-methyl-5-nitroaniline 
• 95-53-4 o-toluidine 
• 5428-54-6 2-methyl-5-nitrophenol 
• 57264-52-5 2-butoxy-1-methyl-4-nitrobenzene 

Downstream Products

• 91289-92-8 4-(2-Amino-4-butoxy-5-methylphenyldiazenyl)-N-methylphthalimid 
• 100514-29-2 3-(2-Amino-4-butoxy-5-methylphenyldiazenyl)benzoesaeure-hydrochlorid 
• 100514-28-1 4-(2-Amino-4-butoxy-5-methylphenyldiazenyl)benzoesaeure-hydrochlorid 
• 100514-16-7 4-(5-Butoxy-6-methyl-2H-benzotriazol-2-yl)benzoesaeure-ethylester 
• 100514-17-8 4-(5-Butoxy-6-methyl-2H-benzotriazol-2-yl)benzoesaeure-methylester 
• 100514-18-9 3-(5-Butoxy-6-methyl-2H-benzotriazol-2-yl)benzoesaeure-ethylester 
• 100514-33-8 4-(5-Butoxy-6-methyl-2H-benzotriazol-2-yl)benzoesaeure 
• 100514-19-0 3-(5-Butoxy-6-methyl-2H-benzotriazol-2-yl)benzoesaeure-methylester 
• 100514-34-9 3-(5-Butoxy-6-methyl-2H-benzotriazol-2-yl)benzoesaeure 

Relevant academic research and scientific papers

Electron Rich Heterocycles as Donor Groups in Fluorescent Dyes

The synthesis of N-methylphthalimides substituted with the donor groups pyrazole, triazole, benzotriazole, and naphthotriazole in position 4 is described (17, 18, 14, 12).The substituent constants of these groups are obtained by alkaline hydrolysis of the corresponding phthalimide dyes.Their solvatochromism in absorption and fluorescence gives information about charge distribution in ground- and excited state.