5-AMINO-3-BROMOBENZONITRILE

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:3-aMino-5-bromobenzonitrile
CAS:49674-16-0
Purity:98%(Min,HPLC) Package:1G;1KG;100KG
Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: Product Name:3-Amino-5-bromobenzonitrile
CAS:49674-16-0
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
Company Name: Alchem Pharmtech,Inc.
Tel: 8485655694
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Products Intro: Product Name:5-Amino-3-bromobenzonitrile
CAS:49674-16-0
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-03241
Company Name: career henan chemical co
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Products Intro: Product Name:5-AMINO-3-BROMOBENZONITRILE
CAS:49674-16-0
Purity:99% Package:1KG;1USD
Company Name: Fuxin Pharmaceutical
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Products Intro: Product Name:3-Amino-5-bromobenzonitrile
CAS:49674-16-0
Purity:99% Package:1kg; 25kg; or larger package as required Remarks:pharmaceutical intermediates;Chemical Intermediate

5-AMINO-3-BROMOBENZONITRILE manufacturers

5-AMINO-3-BROMOBENZONITRILE Basic information
Product Name:5-AMINO-3-BROMOBENZONITRILE
Synonyms:5-AMINO-3-BROMOBENZONITRILE;3-Amino-5-bromobenzonitrile;3-Bromo-5-cyanoaniline;Benzonitrile, 3-amino-5-bromo-
CAS:49674-16-0
MF:C7H5BrN2
MW:197.03
EINECS:
Product Categories:
Mol File:49674-16-0.mol
5-AMINO-3-BROMOBENZONITRILE Structure
5-AMINO-3-BROMOBENZONITRILE Chemical Properties
Boiling point 320.2±22.0 °C(Predicted)
density 1.68±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form powder
pka1.72±0.10(Predicted)
color Off-white
Safety Information
HS Code 2926907090
MSDS Information
5-AMINO-3-BROMOBENZONITRILE Usage And Synthesis
Synthesis
3-Bromo-5-nitrobenzonitrile

49674-15-9

5-AMINO-3-BROMOBENZONITRILE

49674-16-0

General procedure for the synthesis of 5-amino-3-bromobenzonitrile from 3-bromo-5-nitrobenzonitrile: 3-bromo-5-nitrobenzonitrile (3 g, 13.2 mmol) was dissolved in methanol (100 mL) and cooled in an ice water bath. To this solution zinc powder (3.46 g, 52.9 mmol) and acetic acid (6.05 mL, 106 mmol) were added sequentially. Exothermic phenomenon was observed 1 minute after the start of the reaction. After the reaction was carried out for 2 hours, the reaction mixture was filtered through diatomaceous earth and the filtrate was concentrated to give the crude product. The crude product was purified using silica gel chromatography with a hexane solution of 0 to 50% ethyl acetate as eluent. The eluate containing the target product was collected and concentrated by evaporation to give 5-amino-3-bromobenzonitrile (2.1 g, 81% yield). The product was analyzed by high performance liquid chromatography (HPLC): retention time (RT) = 0.80 min (Waters Acquity UPLC BEH C18 column, 1.7 μm, 2.0 × 50 mm, mobile phase acetonitrile/water/0.05% trifluoroacetic acid, gradient elution, detection wavelength = 254 nm); mass spectrum (ES): m/z = 196.9/ 198.9 (79Br/81Br)[M+H]+; 1H NMR (DMSO-d6) δ 7.06-7.09 (m, 1H), 7.04 (t, J=2.0Hz, 1H), 6.87 (dd, J=2.1,1.4Hz, 1H), 5.91 (s, 2H).

References[1] Patent: WO2016/183114, 2016, A1. Location in patent: Page/Page column 61
[2] Patent: WO2009/42694, 2009, A1. Location in patent: Page/Page column 111
[3] Patent: WO2009/42694, 2009, A1. Location in patent: Page/Page column 71
[4] Patent: WO2012/93101, 2012, A1. Location in patent: Page/Page column 241-242
5-AMINO-3-BROMOBENZONITRILE Preparation Products And Raw materials
Raw materials3-Bromo-5-nitrobenzonitrile
Tag:5-AMINO-3-BROMOBENZONITRILE(49674-16-0) Related Product Information
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