5-bromo-2-nitrobenzenamine

5-bromo-2-nitrobenzenamine Suppliers list
Company Name: Shanghai Harvest Chemical Industrial Co., Ltd.  Gold
Tel: 15721252604 17321035817
Email: sales@harvest-chem.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com
Company Name: Shijiazhuang Sdyano Fine Chemical Co., Ltd.  
Tel: 0311-89250318 13582355795
Email: master@sjzsdyn.com
Company Name: Jia Xing Isenchem Co.,Ltd  
Tel: 0573-85285100 18627885956
Email: isenchem@163.com
Company Name: Accela ChemBio Co.,Ltd.  
Tel: 021-50795510 4000665055
Email: marketing@accelachem.com

5-bromo-2-nitrobenzenamine manufacturers

5-bromo-2-nitrobenzenamine Basic information
Product Name:5-bromo-2-nitrobenzenamine
Synonyms:5-bromo-2-nitrobenzenamine;2-Amino-4-bromonitrobenzene;(5-BroMo-2-nitrophenyl)aMine;BenzenaMine, 5-broMo-2-nitro-;5-bromo-2-nitroanline;3-Amino-4-nitrobromobenzene
CAS:5228-61-5
MF:C6H5BrN2O2
MW:217.02
EINECS:
Product Categories:
Mol File:5228-61-5.mol
5-bromo-2-nitrobenzenamine Structure
5-bromo-2-nitrobenzenamine Chemical Properties
Melting point 151-152 °C
Boiling point 331.9±22.0 °C(Predicted)
density 1.812±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
form solid
pka-1.53±0.25(Predicted)
color Light yellow to yellow
InChIInChI=1S/C6H5BrN2O2/c7-4-1-2-6(9(10)11)5(8)3-4/h1-3H,8H2
InChIKeyRMIFLIVHJLREFJ-UHFFFAOYSA-N
SMILESC1(N)=CC(Br)=CC=C1[N+]([O-])=O
Safety Information
HS Code 2921420090
MSDS Information
5-bromo-2-nitrobenzenamine Usage And Synthesis
Synthesis
1-Bromo-4-nitrobenzene

586-78-7

5-bromo-2-nitrobenzenamine

5228-61-5

General procedure for the synthesis of 2-nitro-5-bromoaniline from 1-bromo-4-nitrobenzene: Step 1: Synthesis of 5-bromo-2-nitroaniline (142) [0745] To a solution of ethylene glycol dimethyl ether (170 mL) containing potassium tert-butoxide (21.92 g, 195 mmol) and copper(I) chloride (2.36 g, 23.8 mmol) was added dropwise a solution of 1-bromo-4-nitrobenzene (141, 8.69 g, 43.0 mmol) in DMF (45 mL) at 0 °C and protected by nitrogen, the time of dropwise addition was 50 min. After the dropwise addition, the cooling bath was removed and the reaction mixture was continued to be stirred at room temperature for 4 hours. After completion of the reaction, the reaction solution was diluted with dichloromethane, washed sequentially with aqueous ammonium chloride, dried over anhydrous magnesium sulfate, filtered and concentrated to give the target compound 142 (7.85 g, 84% yield). [0746] 1H NMR (CDCl3) δ (ppm): 7.98 (d, J = 9.2 Hz, 1H), 7.02 (d, J = 2.0 Hz, 1H), 6.82 (dd, J = 9.2, 2.0 Hz, 1H), 6.12 (bs, 2H).

References[1] Patent: WO2007/118137, 2007, A1. Location in patent: Page/Page column 109-110
[2] Journal of the Chemical Society - Perkin Transactions 1, 1999, # 11, p. 1437 - 1444
[3] Patent: WO2016/89830, 2016, A1. Location in patent: Page/Page column 43
[4] Patent: WO2016/89797, 2016, A1. Location in patent: Page/Page column 65
[5] Patent: WO2016/89833, 2016, A1. Location in patent: Page/Page column 42
Tag:5-bromo-2-nitrobenzenamine(5228-61-5) Related Product Information
3-Amino-5-bromopyridine 5-Bromo-2-thiophenecarboxylic acid (5-Bromo-2-nitro-phenyl)-ethyl-amine (5-Bromo-2-nitro-phenyl)-methyl-amine N-(5-Bromo-2-nitrophenyl)-L-proline 5-bromo-2-nitrobenzenamine 5-Bromo-2-nitro-3-acetyl-amino-4-methylbenzoic acid 2-Nitro-3-amino-4-methyl-5-bromobenzoic acid (5-Bromo-2-nitro-phenyl)-(3-chloro-benzyl)-amine (5-Bromo-2-nitro-phenyl)-(2-pyridin-4-yl-ethyl)-amine (5-Bromo-2-nitro-phenyl)-isopropyl-amine (5-Bromo-2-nitro-phenyl)-[2-(4-methyl-piperazin-1-yl)-ethyl]-amine (5-Bromo-2-nitro-phenyl)-(2-piperidin-4-yl-ethyl)-amine (5-Bromo-2-nitro-phenyl)-pyridin-3-ylmethyl-amine AKOS 90585 (5-Bromo-2-nitro-phenyl)-pyridin-2-ylmethyl-amine (5-Bromo-2-nitro-phenyl)-(2-chloro-benzyl)-amine 3,5-Dibromo-4-methyl-2-nitroaniline