2-AMino-3-broMobenzaMide

2-AMino-3-broMobenzaMide Suppliers list
Company Name: ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
Tel: +86-15225627621 +86-13213167925
Email: jiuyitime@fdachem.com
Products Intro: Product Name:2-Amino-3-bromobenzamide
CAS:437998-34-0
Purity:99%min Package:100kg;2.2USD|10kg;6.6USD|1kg;8.8USD
Company Name: Hefei Lbao Physical & Chemical Science Co.,Ltd
Tel: +1-5184799099;
Email: lbaochemicals@gmail.com
Products Intro: Product Name:2-amino-3-bromobenzamide
CAS:437998-34-0
Purity:98% Package:1kg;
Company Name: Alchem Pharmtech,Inc.
Tel: 8485655694
Email: sales@alchempharmtech.com
Products Intro: Product Name:2-AMino-3-broMobenzaMide
CAS:437998-34-0
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-69082
Company Name: CONIER CHEM AND PHARMA LIMITED
Tel:
Email: sales@conier.com
Products Intro: Product Name:2-amino-3-bromobenzamide
CAS:437998-34-0
Package:100g,1kg
Company Name: career henan chemical co
Tel: +86-0371-86658258
Email: factory@coreychem.com
Products Intro: Product Name:BenzaMide, 2-aMino-3-broMo-
CAS:437998-34-0
Purity:98% Package:1KG;1USD

2-AMino-3-broMobenzaMide manufacturers

2-AMino-3-broMobenzaMide Basic information
Product Name:2-AMino-3-broMobenzaMide
Synonyms:BenzaMide, 2-aMino-3-broMo-;2-Amino-3-bromobenzamid;2-AMino-3-broMobenzaMide
CAS:437998-34-0
MF:C7H7BrN2O
MW:215.05
EINECS:
Product Categories:
Mol File:437998-34-0.mol
2-AMino-3-broMobenzaMide Structure
2-AMino-3-broMobenzaMide Chemical Properties
Melting point 249-250 °C
Boiling point 292℃
density 1.698
Fp 131℃
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka15.15±0.50(Predicted)
AppearanceLight yellow to brown Solid
Safety Information
MSDS Information
2-AMino-3-broMobenzaMide Usage And Synthesis
Synthesis
2-AMINO-3-BROMOBENZOIC ACID

20776-51-6

2-AMino-3-broMobenzaMide

437998-34-0

Step A: To a solution of N,N-dimethylformamide (DMF, 5 mL) of 2-amino-3-bromobenzoic acid (0.5 g, 2.3 mmol) was added hydroxybenzotriazole (HOBt, 0.46 g, 3.0 mmol), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC-HCl, 0.53 g, 2.8 mmol), ammonium chloride (0.5 g, 9.7 mmol) and diisopropylethylamine (DIPEA, 1.7 mL, 9.7 mmol) in order at room temperature. 2.8 mmol), ammonium chloride (0.5 g, 9.7 mmol) and diisopropylethylamine (DIPEA, 1.7 mL, 9.7 mmol). The reaction system was purged with nitrogen (N2) and then the reaction was stirred at room temperature for 6 hours. After completion of the reaction, the mixture was poured into water and extracted with ethyl acetate (EtOAc, 3 × 50 mL). The organic phases were combined, washed with saturated saline (2 × 20 mL), dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure. The residue was treated with dichloromethane (DCM, 10 mL) to precipitate, and the precipitate was collected by filtration and dried to afford 2-amino-3-bromobenzamide as a pale pink solid (0.42 g, 84% yield). Liquid chromatography-mass spectrometry (LCMS, ESI) m/z 215/217 ([M+H]+).

References[1] Patent: US2012/53174, 2012, A1. Location in patent: Page/Page column 49
[2] Patent: US2016/168140, 2016, A1. Location in patent: Paragraph 1000
[3] Journal of Agricultural and Food Chemistry, 2015, vol. 63, # 31, p. 6883 - 6889
[4] European Journal of Medicinal Chemistry, 2018, vol. 152, p. 235 - 252
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