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5-Bromo-3-nitro-benzene-1,2-diamine

Product Name
5-Bromo-3-nitro-benzene-1,2-diamine
CAS No.
84752-20-5
Chemical Name
5-Bromo-3-nitro-benzene-1,2-diamine
Synonyms
5-Bromo-3-nitro-benzene-1,2-diamine;1,2-Benzenediamine, 5-bromo-3-nitro-;4-Bromo-6-nitro-1,2-phenylenediamine
CBNumber
CB52445679
Molecular Formula
C6H6BrN3O2
Formula Weight
232.03
MOL File
84752-20-5.mol
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5-Bromo-3-nitro-benzene-1,2-diamine Property

storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
Appearance
Brown to reddish brown Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Biosynth Carbosynth
Product number
FB141535
Product name
5-Bromo-3-nitrobenzene-1,2-diamine
Packaging
250mg
Price
$80
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB141535
Product name
5-Bromo-3-nitrobenzene-1,2-diamine
Packaging
500mg
Price
$140
Updated
2021/12/16
AK Scientific
Product number
Z5178
Product name
5-Bromo-3-nitrobenzene-1,2-diamine
Packaging
1g
Price
$191
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB141535
Product name
5-Bromo-3-nitrobenzene-1,2-diamine
Packaging
1g
Price
$243.75
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB141535
Product name
5-Bromo-3-nitrobenzene-1,2-diamine
Packaging
2g
Price
$415
Updated
2021/12/16
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5-Bromo-3-nitro-benzene-1,2-diamine Chemical Properties,Usage,Production

Synthesis

62554-90-9

84752-20-5

General procedure for the synthesis of 3-nitro-5-bromobenzene-1,2-diamine from 2,6-dinitro-4-bromoaniline: a mixture of 4-bromo-2,6-dinitroaniline (5.5 g, 21.2 mmol) and ammonium sulfide (10.5 mL, 21.2 mmol) in ethanol (150 mL) was heated and reacted for 1 hr at 90 °C. Thin layer chromatography (TLC) monitoring showed incomplete consumption of the feedstock. Ammonium sulfide (10.5 mL, 21.2 mmol) was added and the reaction was continued with stirring at 90 °C for 1 hour. Upon completion of the reaction, the mixture was concentrated and purified by silica gel column chromatography (eluent: petroleum ether/dichloromethane = 1:1) to afford the target compound 3-nitro-5-bromobenzene-1,2-diamine (2.5 g, 51% yield) as a red solid. Liquid chromatography-mass spectrometry (LCMS) analysis results: m/z 230, 232 ([M+H]+).

References

[1] Patent: WO2016/168682, 2016, A2. Location in patent: Paragraph 0288
[2] Patent: US2012/88767, 2012, A1. Location in patent: Page/Page column 13; 15; 19
[3] Analytical Chemistry, 1983, vol. 55, # 6, p. 963 - 965

5-Bromo-3-nitro-benzene-1,2-diamine Preparation Products And Raw materials

Raw materials

Preparation Products

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5-Bromo-3-nitro-benzene-1,2-diamine Suppliers

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