Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Hydrocarbons and derivatives >  Hydrocarbon nitrification >  4-Bromo-5-fluoro-2-nitrotoluene

4-Bromo-5-fluoro-2-nitrotoluene

Basic information Safety Supplier Related

4-Bromo-5-fluoro-2-nitrotoluene Basic information

Product Name:
4-Bromo-5-fluoro-2-nitrotoluene
Synonyms:
  • 4-Bromo-5-fluoro-2-nitortoluene
  • 2-Nitro-4-Bromo-5-Fluorotoluene
  • 4-BROMO-3-FLUORO-6-NITROTOLUENE
  • 4-BROMO-5-FLUORO-2-NITROTOLUENE
  • 1-Bromo-2-fluoro-4-methyl-5-nitro-benzene
  • Benzene,1-broMo-2-fluoro-4-Methyl-5-nitro-
  • 1-Bromo-2-fluoro-4-methyl-5-n
  • 4-Bromo-5-fluoro-2-nitrotoluene 99%
CAS:
224185-19-7
MF:
C7H5BrFNO2
MW:
234.02
EINECS:
625-785-2
Product Categories:
  • Nitrogen Compounds
  • Organic Building Blocks
  • Aromatic Hydrocarbons (substituted) & Derivatives
  • Halogen toluene
  • Miscellaneous
  • Nitro Compounds
Mol File:
224185-19-7.mol
More
Less

4-Bromo-5-fluoro-2-nitrotoluene Chemical Properties

Melting point:
59-63°C
Boiling point:
266.6±35.0 °C(Predicted)
Density 
1.696±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
color 
Cream
InChIKey
MTTNTJRJOFVWSY-UHFFFAOYSA-N
CAS DataBase Reference
224185-19-7(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-36-36/37/38
Safety Statements 
26-36/37-36
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29049090

MSDS

More
Less

4-Bromo-5-fluoro-2-nitrotoluene Usage And Synthesis

Chemical Properties

pale yellow powder

Synthesis

2-Fluoro-4-methyl-5-nitro-aniline (1.85 g, 10.90 mmol) was suspended in concentrated hydrobromic acid (22 ml_) and cooled to 0 ℃. Solution of sodium nitrite (0.83 g, 12.00 mmol) in water (3.6 ml_) was added dropwise while maintaining the temperature at 0-5 °C. After stirring for 15 min, the mixture was filtered through a cotton pad and slowly poured into a solution of cuprous oxide (2.60 g, 17.5 mmol) and concentrated hydrobromic acid (20 ml) at 0 °C. After stirring overnight, the reaction mixture was diluted with EtOAc, washed with 10 % aq NaOH and 5percent aq Na2S2Os successively, dried over MgSO4, filtered and concentrated. The residue was purified by column chromatography (ethyl acetate: hexane; 2:98) to afford 1-Bromo-2-fluoro-4- methyl-5-nitro-benzene as a colorless oil (2.30 g, 91 %).

References

[1] Patent: WO2003/99824, 2003, A1. Location in patent: Page 32
[2] Patent: WO2003/99275, 2003, A1. Location in patent: Page 65
[3] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 2, p. 457 - 460
[4] Patent: WO2015/54572, 2015, A1. Location in patent: Page/Page column 247
[5] Patent: US2004/224973, 2004, A1. Location in patent: Page 21

4-Bromo-5-fluoro-2-nitrotolueneSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Beijing Ouhe Technology Co., Ltd
Tel
010-010-82967028 13522913783
Email
2355560935@qq.com