4-BroMo-5-nitrobenzene-1,2-diaMine

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4-BroMo-5-nitrobenzene-1,2-diaMine Basic information
Product Name:4-BroMo-5-nitrobenzene-1,2-diaMine
Synonyms:4-BroMo-5-nitrobenzene-1,2-diaMine;1,2-Benzenediamine, 4-bromo-5-nitro-
CAS:113269-07-1
MF:C6H6BrN3O2
MW:232.03
EINECS:
Product Categories:
Mol File:113269-07-1.mol
4-BroMo-5-nitrobenzene-1,2-diaMine Structure
4-BroMo-5-nitrobenzene-1,2-diaMine Chemical Properties
Boiling point 394.1±37.0 °C(Predicted)
density 1.901±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
pka1.46±0.10(Predicted)
Safety Information
MSDS Information
4-BroMo-5-nitrobenzene-1,2-diaMine Usage And Synthesis
Synthesis
N,N'-(4-bromo-5-nitro-1,2-phenylene)bis(4-methylbenzenesulfonamide)

113269-05-9

4-BroMo-5-nitrobenzene-1,2-diaMine

113269-07-1

General procedure for the synthesis of 4-bromo-5-nitrobenzene-1,2-diamine from N,N'-(4-bromo-5-nitro-1,2-phenylene)bis(4-methylbenzenesulfonamide): N,N'-(4-bromo-5-nitro-1,2-phenylene)bis(4-methylbenzenesulfonamide) (0.92 g. 1.71 mmol) was placed in a 10 mL round bottom flask. 90% sulfuric acid (2 mL) was added slowly and the reaction mixture was placed in an oil bath at 85°C with stirring and reflux for 2 hours. Upon completion of the reaction, the mixture was removed and cooled to room temperature and subsequently poured into 50 mL of water. The pH was adjusted to 9 with ammonia, at which point a red solid precipitated. After the mixture was cooled, filtration was carried out and the solid was washed twice with cold water. 4-Bromo-5-nitrobenzene-1,2-diamine (0.34 g, 86.8% yield) was finally obtained.

References[1] Heterocycles, 1987, vol. 26, # 9, p. 2433 - 2442
[2] Patent: CN108341791, 2018, A. Location in patent: Paragraph 0013; 0014; 0017
4-BroMo-5-nitrobenzene-1,2-diaMine Preparation Products And Raw materials
Raw materialsN,N'-(4-bromo-5-nitro-1,2-phenylene)bis(4-methylbenzenesulfonamide)
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