ChemicalBook > Product Catalog >Organic Chemistry >Organic fluorine compound >Fluorotoluene series >2-Chloro-5-iodobenzotrifluoride

2-Chloro-5-iodobenzotrifluoride

2-Chloro-5-iodobenzotrifluoride Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com
Company Name: TCI (Shanghai) Development Co., Ltd.  
Tel: 021-67121386
Email: Sales-CN@TCIchemicals.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

2-Chloro-5-iodobenzotrifluoride manufacturers

2-Chloro-5-iodobenzotrifluoride Basic information
Product Name:2-Chloro-5-iodobenzotrifluoride
Synonyms:2-Chloro-5-iodobenzotrifluoride;2-chloro-5-iodo-trifluoromethylbenzene;2-Chloro-5-iodobenzotrifluoride >;5-iodo-2-chlorobenzotrifluoride;Benzene, 1-chloro-4-iodo-2-(trifluoromethyl)-;1-chloro-4-iodo-2-(trifluoromethyl)benzene
CAS:260355-20-2
MF:C7H3ClF3I
MW:306.45
EINECS:
Product Categories:
Mol File:260355-20-2.mol
2-Chloro-5-iodobenzotrifluoride Structure
2-Chloro-5-iodobenzotrifluoride Chemical Properties
Melting point 28 °C
Boiling point 235 ºC
density 1.952
Fp 28 °C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form powder to lump
color White to Light yellow
InChIKeyMCIFWVOVVPVBRJ-UHFFFAOYSA-N
Safety Information
HS Code 2903998090
MSDS Information
2-Chloro-5-iodobenzotrifluoride Usage And Synthesis
Chemical Propertiesliquid
Synthesis
4-iodo-2-(trifluoroMethyl)phenol

1132942-88-1

2-Chloro-5-iodobenzotrifluoride

260355-20-2

General procedure for the synthesis of 2-chloro-5-iodobenzotrifluoride from 2-trifluoromethyl-4-iodophenol: 4-iodo-2-trifluoromethylphenol (10 mmol) obtained in 1.1 was dissolved in 20 mL of N,N-dimethylformamide (DMF). Subsequently, phosphorous trichloride (10.5 mmol) was added, and the reaction system was placed in a microwave reactor, heated to 130 °C, and kept for 1 hour. After the reaction was completed, the system was cooled to room temperature, 30 mL of water was added and stirred for 10 minutes. The reaction mixture was extracted with 30 mL of dichloromethane and the organic phase was dried with anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. Purification by fast column chromatography using petroleum ether as eluent gave 2.1 g of light yellow solid 1-chloro-4-iodo-2-trifluoromethylbenzene in 69% yield.

References[1] Patent: CN108184888, 2018, A. Location in patent: Paragraph 0014
[2] Patent: CN108338175, 2018, A. Location in patent: Paragraph 0019
[3] Patent: CN108353907, 2018, A. Location in patent: Paragraph 0015-0016
[4] Patent: CN108353920, 2018, A. Location in patent: Paragraph 0014
[5] Patent: CN108432777, 2018, A. Location in patent: Paragraph 0016
2-Chloro-5-iodobenzotrifluoride Preparation Products And Raw materials
Raw materials4-iodo-2-(trifluoroMethyl)phenol-->trichlorophosphate-->N,N-Dimethylformamide
Tag:2-Chloro-5-iodobenzotrifluoride(260355-20-2) Related Product Information
Fluorolube grease, GR-362 Benzene Benzotrifluoride λ-Cyhalothrin Epichlorohydrin 2-Chloro-5-nitrobenzotrifluoride 4-Chlorotoluene 3-Fluorobenzotrifluoride 2-Chloro-5-trifluoromethylpyridine Allylbenzene 2-Methylbenzotrifluoride 1,4-Bis(trifluoromethyl)-benzene Ethylbenzene Benzyl chloride Difluorochloromethane Chloroacetic acid 3-Iodobenzotrifluoride Trifluoromethyl