65644-51-1

Upstream product

• 122-04-3 4-nitro-benzoyl chloride 
• 23451-96-9 2-amino-5-methylthiophenol 
• 873-74-5 4-Aminobenzonitrile 
• 19759-66-1 2-amino-6-cyanobenzthiazole 
• 14543-45-4 4-amino-3-mercaptobenzoic acid 
• 555-16-8 4-nitrobenzaldehdye 

Downstream Products

• 13127-94-1 2-(4-aminophenyl)benzo[d]thiazole-6-carboxylic acid 
• 875846-26-7 2-(4-nitrophenyl)benzothiazole-6-carbonyl chloride 
• 934704-63-9 C₂₀H₁₀FN₃O₂S₂ 
• 934704-64-0 C₂₀H₁₀(OCH₃)N₃O₂S₂ 
• 909904-76-3 C₂₀H₁₃N₃S₂ 
• 934704-65-1 C₂₀H₁₂ClN₃S₂ 
• 934704-66-2 C₂₀H₁₂FN₃S₂ 
• 945920-01-4 2-(4-nitro-phenyl)-benzothiazole-6-carboxylic acid methyl ester 
• 95-22-7 4-(6-methyl-[2,6']bibenzothiazolyl-2'-yl)-aniline 
• 855266-37-4 6-methyl-2'-(4-nitro-phenyl)-[2,6']bibenzothiazolyl 
• 73302-00-8 4-(6-methyl-[2,6';2',6'']terbenzothiazol-2''-yl)-aniline 

Relevant academic research and scientific papers

A convenient route to 2-substituted benzothiazole-6-carboxylic acids using nitrobenzene as oxidant

Various substituted benzothiazole-6-carboxylic acids (4a-i) have been prepared by the condensation of 4-amino-3-mercaptobenzoic acid and aldehydes in nitrobenzene as oxidant. Compound 4i was found to be a good candidate as an inhibitor of ss-hematin formation in vitro.

ADSORPTION AND LUMINESCENCE IN THE SERIES OF 2-PHENYLBENZOTHIAZOLE AND RELATED COMPOUNDS

Electronic transitions in the molecules of derivatives of 2-phenylbenzothiazole containing substituents in the annelated and 2-phenyl nuclei proceed with the participation of different excited states with charge transfer, their contribution depending on t