ChemicalBook > Product Catalog >Organic Chemistry >Organic fluorine compound >Fluorotoluene series >1-Bromo-3-fluoro-5-methylbenzene

1-Bromo-3-fluoro-5-methylbenzene

1-Bromo-3-fluoro-5-methylbenzene Suppliers list
Company Name: Shanghai Harvest Chemical Industrial Co., Ltd.  Gold
Tel: 15721252604 17321035817
Email: sales@harvest-chem.com
Company Name: FUXIN QINGJISHENG SCIENCE AND TECHNOLOGY CO.,LID  Gold
Tel: 15940530539 15396717197
Email: 361811402@qq.com
Company Name: Shanghai F.R. Chemical Technology Co.,Ltd  Gold
Tel: 021-52230662 13795399395
Email: seaman79@126.com
Company Name: Lianhe Aigen Pharmatech Co.,Ltd.  Gold
Tel: 18918657159
Email: sales-Aigen@lianhetech.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com

1-Bromo-3-fluoro-5-methylbenzene manufacturers

1-Bromo-3-fluoro-5-methylbenzene Basic information
Product Name:1-Bromo-3-fluoro-5-methylbenzene
Synonyms:3-BROMO-5-FLUOROTOLUENE;3-Bromo-5-fluorotoluene 98%;3-Bromo-5-fluorotoluene98%;3-Bromo-5-Fluorotoluene/5-Bromo-3-Fluorotoluene;Fluoro-5-bromotoluene;3-Bromine-5-Fluoride Toluene;Benzene, 1-bromo-3-fluoro-5-methyl-;1-BROMO-3-FLUORO-5-METHYLBENZENE
CAS:202865-83-6
MF:C7H6BrF
MW:189.02
EINECS:606-501-6
Product Categories:Fluorine series;Fluorobenzene;Halogen toluene;Bromine Compounds;Fluorine Compounds
Mol File:202865-83-6.mol
1-Bromo-3-fluoro-5-methylbenzene Structure
1-Bromo-3-fluoro-5-methylbenzene Chemical Properties
Boiling point 183.4±20.0 °C(Predicted)
density 1.498±0.06 g/cm3(Predicted)
storage temp. 2-8°C
form Liquid
color Colorless
InChIInChI=1S/C7H6BrF/c1-5-2-6(8)4-7(9)3-5/h2-4H,1H3
InChIKeyCTNFNUQREIIROB-UHFFFAOYSA-N
SMILESC1(Br)=CC(C)=CC(F)=C1
CAS DataBase Reference202865-83-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 10-36/37/38-36-22
Safety Statements 16-26-36
RIDADR 1993
HazardClass IRRITANT
HS Code 2903998090
MSDS Information
1-Bromo-3-fluoro-5-methylbenzene Usage And Synthesis
Uses3-Bromo-5-fluorotoluene is an important halotoluene compound used as a structural component of many organic heterocyclic compounds. It has reactive groups, bromine and fluorine atoms, which can be used in substitution reactions.
Synthesis2-Bromo-6-fluoro-4-methylaniline (11.2 g, 55 mmol), diluted hydrochloric acid (28.5 mL, 6 M) and acetonitrile (300 mL) were added to a 500 mL single-neck flask, then to the mixture in flask was added dropwise slowly a solution of sodium nitrite (5.69 g, 82.4 mmol) in water (40 mL) at 0 °C. After the addition, the reaction mixture was stirred at 0 °C for 1 h; then a solution of potassium iodide (18.3 g, 110 mmol) was added to the flask in water (30 mL). After the addition, the mixture was stirred at 0 °C for 0.5 h, then stirred at rt overnight. The reaction mixture was added saturated aqueous sodium sulfite (300 mL), and the resulting mixture was concentrated in vacuo to remove acetonitrile. The residue was extracted with ethyl acetate (100 mL x 2), combining the organic layers. The combined organic layers were washed with saturated brine (100 mL), dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated in vacuo. The residue was purified by silica-gel column chromatography (ethyl acetate/petroleum ether (v/v) = 1/100) to give 1-Bromo-3-fluoro-5-methylbenzene as a white solid (13.2 g, 76%).
References[1] Patent: WO2017/36404, 2017, A1. Location in patent: Page/Page column 124
Tag:1-Bromo-3-fluoro-5-methylbenzene(202865-83-6) Related Product Information
4-Chlorobenzotrifluoride p-Fluorotoluene 2-Fluorotoluene 4-Bromotoluene 3-Fluorobenzotrifluoride Benzotrifluoride Fluorine 2-Bromo-6-fluorotoluene 3-Bromo-5-fluorobenzotrifluoride 2-Fluoro-5-bromobenzotrifluoride 3-Bromo-2-fluorotoluene 4-Bromo-3-fluorotoluene 2-Bromobenzotrifluoride Bromine 2-Bromo-5-fluorotoluene 2'-Bromo-4'-(trifluoromethyl)acetanilide 98 4-Bromo-3-(trifluoromethyl)aniline 3-Amino-5-bromobenzotrifluoride