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3-Bromo-5-nitrobenzene-1,2-diamine

3-Bromo-5-nitrobenzene-1,2-diamine Suppliers list
Company Name: Jinan Carbotang Biotech Co.,Ltd.
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Products Intro: Product Name:3-BROMO-5-NITROBENZENE-1,2-DIAMINE
CAS:69399-60-6
Purity:98% Package:5KG;1KG
Company Name: Shanghai Gubang New Materail Technology Co. LTD
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Products Intro: Product Name:3-Bromo-5-nitro-benzene-1,2-diamine
CAS:69399-60-6
Purity:0.97 Package:1 g 2 g, 5 g, 10 g, 1000 g
Company Name: Santai Labs, Inc.  
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Products Intro: Product Name:3-bromo-5-nitrobenzene-1,2-diamine
CAS:69399-60-6
Purity:97% HPLC Package:25G;100G;1kg;25kg
Company Name: LinkChem Co.,Ltd.  
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Products Intro: Product Name:3-bromo-5-nitrobenzene-1,2-diamine
CAS:69399-60-6
Purity:90% Package:1g;5g;10g;100g
Company Name: Jinan Kabotang Biological Technology Co.,Ltd.  
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Products Intro: Product Name:3-BROMO-5-NITROBENZENE-1,2-DIAMINE
CAS:69399-60-6
Purity:98% HPLC Package:1kg
3-Bromo-5-nitrobenzene-1,2-diamine Basic information
Product Name:3-Bromo-5-nitrobenzene-1,2-diamine
Synonyms:3-BROMO-5-NITROBENZENE-1,2-DIAMINE;3-Bromo-5-nitro-1,2-diaminobenzene;1,2-Benzenediamine, 3-bromo-5-nitro-;Guaiacol Impurity 19-d5
CAS:69399-60-6
MF:C6H6BrN3O2
MW:232.03
EINECS:
Product Categories:
Mol File:69399-60-6.mol
3-Bromo-5-nitrobenzene-1,2-diamine Structure
3-Bromo-5-nitrobenzene-1,2-diamine Chemical Properties
Melting point 203-205 °C
Boiling point 426.5±40.0 °C(Predicted)
density 1.901±0.06 g/cm3(Predicted)
pka0.81±0.10(Predicted)
Safety Information
MSDS Information
3-Bromo-5-nitrobenzene-1,2-diamine Usage And Synthesis
SynthesisSodium sulfide nonahydrate (96 g, 400 mmol) and sulfur (12.8 g, 400 mmol) in a mixture of water and ethanol was heated at reflux under nitrogen for 1 h. The solution was added to a stirred suspension of 2-bromo-4,6-dinitrobenzenamine (104.8 g, 400 mmol) and ammonium chloride (20.8 g, 400 mmol) in a solution of 400 mL of water and 700 mL of ethanol. The mixture was stirred at 65° C for 30 min. Then 400 mL of 2N NaOH solution was added dropwise during 30 min and the mixture was then stirred for 15 minutes at 65° C. After cooling, the mixture was poured onto a mixture of 2N HCl (400 mL), 1 kg ice and 1 L of water, stirred for 15 min to complete the reaction and extracted with ethyl acetate (1 L*3). The combined organic layers were dried over sodium sulphate and evaporated to give the crude product (3-Bromo-5-nitrobenzene-1,2-diamine) (90 g, 97%) as a rust-colored solid, which was used for the next step without further purification.3-Bromo-5-nitrobenzene-1,2-diamine
3-Bromo-5-nitrobenzene-1,2-diamine Preparation Products And Raw materials
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