ChemicalBook > Product Catalog >Organic Chemistry >Nitrogen Compounds >5-Bromo-3-methyl-benzene-1,2-diamine

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

5-Bromo-3-methyl-benzene-1,2-diamine Suppliers list
Company Name: Nanjing Qishi Biotechnology Co. Ltd.  Gold
Tel: 19822610310
Email: 3122922726@qq.com
Company Name: Heze Bona Medical Technology Co., LTD  Gold
Tel: 15865805009
Email: 15865805009@139.com
Company Name: Wuhan Chemwish Technology Co., Ltd  
Tel: 86-027-67849912
Email: sales@chemwish.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-3-methyl-benzene-1,2-diamine manufacturers

5-Bromo-3-methyl-benzene-1,2-diamine Basic information
Product Name:5-Bromo-3-methyl-benzene-1,2-diamine
Synonyms:5-BROMO-3-METHYL-1,2-BENZENEDIAMINE;5-Bromo-3-methyl-1,2-diaminobenzene;1,2-Benzenediamine, 5-bromo-3-methyl-;3-methyl-5-bromo-o-phenylenediamine;5-Bromo-3-methyl-benzene-1,2-diamine
CAS:76153-06-5
MF:C7H9BrN2
MW:201.06
EINECS:
Product Categories:pharmacetical
Mol File:76153-06-5.mol
5-Bromo-3-methyl-benzene-1,2-diamine Structure
5-Bromo-3-methyl-benzene-1,2-diamine Chemical Properties
Melting point 63 °C
Boiling point 298.8±35.0 °C(Predicted)
density 1.589±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka3.31±0.10(Predicted)
AppearanceBrown to dark brown Solid
InChIInChI=1S/C7H9BrN2/c1-4-2-5(8)3-6(9)7(4)10/h2-3H,9-10H2,1H3
InChIKeyUOFSLKHZOPVGHG-UHFFFAOYSA-N
SMILESC1(N)=CC(Br)=CC(C)=C1N
CAS DataBase Reference76153-06-5
Safety Information
HazardClass IRRITANT
HS Code 2921599090
MSDS Information
5-Bromo-3-methyl-benzene-1,2-diamine Usage And Synthesis
Uses5-Bromo-3-methylbenzene-1,2-diamine is used as an intermediate in organic synthesis.
Synthesis
4-Bromo-2-methyl-6-nitroaniline

77811-44-0

5-BROMO-3-METHYL-BENZENE-1,2-DIAMINE

76153-06-5

Step 1: Stannous chloride (SnCl2, 5.0 g, 26.1 mmol) was added to an ethanol (EtOH, 20 mL) suspension of 4-bromo-2-methyl-6-nitroaniline (2.0 g, 8.7 mmol). The reaction mixture was heated to reflux for 14 h, followed by cooling to room temperature and vacuum concentration. The residue was diluted with ethyl acetate (EtOAc, 100 mL) and partitioned between saturated aqueous sodium bicarbonate (NaHCO3) solution (200 mL) and water. The resulting slurry was filtered through a Celite pad and the wet filter cake was washed with ethyl acetate (3 x 50 mL). The filtrate was washed sequentially with saturated aqueous sodium bicarbonate, water, and brine, dried over anhydrous magnesium sulfate (MgSO4), filtered, and concentrated in vacuum to give 1.27 g (72% yield) of 5-bromo-3-methylbenzene-1,2-diamine (72) as a yellow oil: mass spectrum (ESI) m/z = 201.1 [M + 1]+.

References[1] Patent: WO2013/26914, 2013, A1. Location in patent: Page/Page column 130
[2] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 11, p. 3072 - 3076
[3] Patent: US2005/54655, 2005, A1. Location in patent: Page/Page column 15-16
[4] Patent: US2004/44203, 2004, A1. Location in patent: Page 28
[5] Chemische Berichte, 1884, vol. 17, p. 776
5-Bromo-3-methyl-benzene-1,2-diamine Preparation Products And Raw materials
Raw materials4-Bromo-2-methyl-6-nitroaniline-->Ethanol-->Stannous chloride
Preparation Products2,3-Quinoxalinedione, 7-bromo-1,4-dihydro-5-methyl--->Quinoxaline, 7-bromo-5-methyl- (9CI)
Tag:5-Bromo-3-methyl-benzene-1,2-diamine(76153-06-5) Related Product Information
1-Acetyl-5-bromo-7-nitroindoline 5-Bromo-3,4-dimethylbenzene-1,2-diamine 5-Bromo-3-methyl-benzene-1,2-diamine 4-Bromo-2,3-dimethyl-6-nitroaniline 5-Bromo-7-nitroindoline 4-Bromo-2-methyl-6-nitroaniline 2-Amino-5-Bromo-3-Nitrobenzotrifluoride 2-amino-5-bromo-3-nitrobenzoic acid CGP 78608 HYDROCHLORIDE 5-BROMO-2,3-DIAMINOBENZOTRIFLUORIDE 4-bromo-3-fluoro-2-methyl-6-nitroaniline 5-Bromo-2-nitro-3-acetyl-amino-4-methylbenzoic acid 2-NITRO-3-AMINO-4-METHYL-5-BROMOBENZOIC ACID 1-Acetyl-5-bromoindolin-7-amine 1-(4-Bromo-2-methyl-6-nitrophenyl)-1H-pyrrole CGP 78608 N'-(4-BROMO-2-METHYL-6-NITROPHENYL)-N,N-DIMETHYLIMINOFORMAMIDE 5-BROMO-3-ETHYLBENZENE-1,2-DIAMINE