62101-45-5

Basic information

• Product Name: 1,4-Naphthalenedione, 2-[(4-bromophenyl)amino]-3-chloro-
• CAS NO: 62101-45-5
• Molecular Formula: C16H9BrClNO2
• Molecular Weight: 362.61
• Mol File: 62101-45-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,4-Naphthalenedione, 2-[(4-bromophenyl)amino]-3-chloro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Naphthalenedione, 2-[(4-bromophenyl)amino]-3-chloro-(62101-45-5)
• EPA Substance Registry System: 1,4-Naphthalenedione, 2-[(4-bromophenyl)amino]-3-chloro-(62101-45-5)

Safety Data

• Hazardous Substances Data: 62101-45-5(Hazardous Substances Data)

Upstream product

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

Downstream Products

• 172507-76-5 6-(4-Bromo-phenylamino)-10-chloro-9-methyl-benzo[a]phenothiazin-5-one 
• 172507-77-6 6-(4-Bromo-phenylamino)-8-chloro-11-methoxy-benzo[a]phenothiazin-5-one 
• 172507-75-4 6-(4-Bromo-phenylamino)-9-phenoxy-benzo[a]phenothiazin-5-one 
• 73518-83-9 6-(4-bromo-anilino)-12H-benzo[a]phenothiazin-5-ol 
• 73518-90-8 (4-bromo-phenyl)-(5-methoxy-12H-benzo[a]phenothiazin-6-yl)-amine 
• 73518-86-2 6-(4-bromo-anilino)-9-methyl-12H-benzo[a]phenothiazin-5-ol 
• 73518-87-3 6-(4-bromo-anilino)-10-chloro-12H-benzo[a]phenothiazin-5-ol 
• 73518-84-0 6-(4-bromo-anilino)-9-chloro-12H-benzo[a]phenothiazin-5-ol 
• 73518-85-1 9-bromo-6-(4-bromo-anilino)-12H-benzo[a]phenothiazin-5-ol 
• 73518-93-1 (4-bromo-phenyl)-(5-methoxy-9-methyl-12H-benzo[a]phenothiazin-6-yl)-amine 
• 73518-91-9 (4-bromo-phenyl)-(9-chloro-5-methoxy-12H-benzo[a]phenothiazin-6-yl)-amine 
• 73518-94-2 (4-bromo-phenyl)-(10-chloro-5-methoxy-12H-benzo[a]phenothiazin-6-yl)-amine 
• 73518-92-0 (9-bromo-5-methoxy-12H-benzo[a]phenothiazin-6-yl)-(4-bromo-phenyl)-amine 
• 73518-89-5 6-(4-bromo-anilino)-10-ethoxy-12H-benzo[a]phenothiazin-5-ol 

Relevant articles and documents

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

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