62101-45-5

Upstream product

• 117-80-6 2,3-Dichloro-1,4-naphthoquinone 
• 106-40-1 4-bromo-aniline 
• 75-15-0 carbon disulfide 
• 1090-16-0 2-chloro-3-(phenylamino)naphthalene-1,4-dione 
• 7726-95-6 bromine 
• 605-69-6 1-hydroxy-2,4-dinitronaphthalene 
• 64505-67-5 2-((4-bromophenyl)amino)naphthalene-1,4-dione 

Downstream Products

• 73518-95-3 (4-bromo-phenyl)-(5-methoxy-10-trifluoromethyl-12H-benzo[a]phenothiazin-6-yl)-amine 
• 73518-88-4 6-(4-bromo-anilino)-10-trifluoromethyl-12H-benzo[a]phenothiazin-5-ol 
• 73518-96-4 (4-bromo-phenyl)-(10-ethoxy-5-methoxy-12H-benzo[a]phenothiazin-6-yl)-amine 
• 73518-89-5 6-(4-bromo-anilino)-10-ethoxy-12H-benzo[a]phenothiazin-5-ol 
• 73518-92-0 (9-bromo-5-methoxy-12H-benzo[a]phenothiazin-6-yl)-(4-bromo-phenyl)-amine 
• 73518-94-2 (4-bromo-phenyl)-(10-chloro-5-methoxy-12H-benzo[a]phenothiazin-6-yl)-amine 
• 73518-91-9 (4-bromo-phenyl)-(9-chloro-5-methoxy-12H-benzo[a]phenothiazin-6-yl)-amine 
• 73518-93-1 (4-bromo-phenyl)-(5-methoxy-9-methyl-12H-benzo[a]phenothiazin-6-yl)-amine 
• 73518-85-1 9-bromo-6-(4-bromo-anilino)-12H-benzo[a]phenothiazin-5-ol 
• 73518-84-0 6-(4-bromo-anilino)-9-chloro-12H-benzo[a]phenothiazin-5-ol 
• 73518-87-3 6-(4-bromo-anilino)-10-chloro-12H-benzo[a]phenothiazin-5-ol 
• 73518-86-2 6-(4-bromo-anilino)-9-methyl-12H-benzo[a]phenothiazin-5-ol 
• 73518-90-8 (4-bromo-phenyl)-(5-methoxy-12H-benzo[a]phenothiazin-6-yl)-amine 
• 73518-83-9 6-(4-bromo-anilino)-12H-benzo[a]phenothiazin-5-ol 

Relevant academic research and scientific papers

Crystallographic evidence for resonance assisted H-Bonding effect in selective colorimetric detection of cyanide by arylamino-naphthoquinones

Five new chemo-receptors, based on arylamino-naphthoquinone, possessing electron donating and electron withdrawing substituents have been prepared by single step green method. These receptors are found to be highly selective and sensitive towards cyanide

Composition for Distructing Microalgae

The present invention relates to a composition for destroying microalgae, more specifically, to a composition for destroying microalgae containing naphthoquinone compounds having a specific exchange group. The composition for destroying microalgae, according to the present invention, can prevent green tide and red tide by being processed in areas such as cultivation facilities for microalgae, areas in which the green tide or the red tide occur, or areas expected to occur the green tide or the red tide.

Spectroscopic and theoretical studies on the nucleophilic substitution of 2,3-dichloronaphthoquinone with para-substituted anilines in solid state via initial charge transfer complexation

Various spectroscopy techniques (UV-Vis, DRS, FT-IR, 1H NMR, LC-MS) and theoretical computations have been employed to investigate the mechanism of the nucleophilic substitution reaction of 2,3- dichloronaphthoquinone (DCNQ) with para-substitut

Iodination and chlorination of 2-/4-arylamino-1,4-/1,2-naphthoquinones with alkylhalides and DMSO

2-/4-Arylamino-1,4-/1,2-naphthoquinones 10/13 are chlorinated with tert-butylbromide, DMSO and calcium chloride to give 2-/4-arylamino-3-chloro-1,4-/1,2-naphthoquinones 11A/14A. The iodination with tert-butylbromide, DMSO and potassium iodide give 2-/4-arylamino-3-iodo-1,4-/1,2-naphthoquinones 11C/14C.