2-BroMo-4-Methyl-1-nitro-benzene

2-BroMo-4-Methyl-1-nitro-benzene Suppliers list
Company Name: Zhuhai Aobokai Biomedical Technology Co., Ltd.  Gold
Tel: 400-0628126
Email: sales-team@aobchem.com.cn
Company Name: Shanghai Harvest Chemical Industrial Co., Ltd.  
Tel: 15721252604 17321035817
Email: sales@harvest-chem.com
Company Name: Wuhan ariel chemical Co., LTD.  
Tel: 18986259541 18986259541
Email: sales@3stc.com
Company Name: Yancheng Orgunion Pharmaceutical Sci & Tech Co., Ltd.  
Tel: 0515-89701588 13770166955
Email: orgunion@orgunion.com
Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 18317119277
Email: product02@bidepharm.com

2-BroMo-4-Methyl-1-nitro-benzene manufacturers

2-BroMo-4-Methyl-1-nitro-benzene Basic information
Product Name:2-BroMo-4-Methyl-1-nitro-benzene
Synonyms:Benzene, 2-bromo-4-methyl-1-nitro-;2-bromo-4-methyl-1-nitro-benzene - [B86692]
CAS:40385-54-4
MF:C7H6BrNO2
MW:216.03
EINECS:
Product Categories:
Mol File:40385-54-4.mol
2-BroMo-4-Methyl-1-nitro-benzene Structure
2-BroMo-4-Methyl-1-nitro-benzene Chemical Properties
Melting point 37.8°C
Boiling point 269°C (rough estimate)
density 1.6841 (rough estimate)
refractive index 1.6120 (estimate)
storage temp. Sealed in dry,Room Temperature
Safety Information
MSDS Information
2-BroMo-4-Methyl-1-nitro-benzene Usage And Synthesis
Uses3-Bromo-4-nitrotoluene is a compound involved in the synthesis of novel phenylalanine-based amino acids as kainate receptor ligands.
Synthesis
2-Bromo-4-methylaniline

583-68-6

2-BroMo-4-Methyl-1-nitro-benzene

40385-54-4

General procedure for the synthesis of 2-bromo-4-methyl-1-nitrobenzene from 2-bromo-4-methylaniline: 77% 3-chloroperoxybenzoic acid (150 mmol, 33.62 g) was added to a solution of 2-bromo-4-methylaniline (30 mmol, 5.56 g) in toluene (100 mL), and the reaction mixture was heated and refluxed for 6 hours. After completion of the reaction, the mixture was cooled to room temperature and filtered. The filtrate was washed sequentially with 10% sodium hydroxide solution (2 x 100 mL) and saturated saline (100 mL), and the organic phase was dried with anhydrous sodium sulfate. The solvent was removed by evaporation under reduced pressure and the resulting residue was purified by fast column chromatography.

References[1] Journal of the American Chemical Society, 2005, vol. 127, # 13, p. 4609 - 4624
[2] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 22, p. 5568 - 5572
[3] Collection of Czechoslovak Chemical Communications, 1967, vol. 32, # 1, p. 382 - 397
[4] Journal of medicinal chemistry, 1971, vol. 14, # 11, p. 1113 - 1115
[5] Tetrahedron Letters, 1992, vol. 33, # 33, p. 4799 - 4802
2-BroMo-4-Methyl-1-nitro-benzene Preparation Products And Raw materials
Raw materials2-Bromo-4-methylaniline-->3-Chloroperoxybenzoic acid-->Toluene
Preparation ProductsMethyl 3-broMo-4-nitrobenzoate-->2-Bromo-4-methylaniline
Tag:2-BroMo-4-Methyl-1-nitro-benzene(40385-54-4) Related Product Information
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