(DIFLUOROMETHOXY)BENZENE

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Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: CAS:458-92-4
Purity:98% HPLC Package:5MG;10MG;50MG;100MG,1G,5G
Company Name: Changzhou Ansciep Chemical Co., Ltd.
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Products Intro: Product Name:Difluoromethoxybenzene
CAS:458-92-4
Purity:0.99 Package:100g, 500g, 1kg, 25kg, 50kg, 200kg Remarks:Good quality; Large stock; Hot sale
Company Name: Nanjing Dolon Biotechnology Co.,Ltd.
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Products Intro: CAS:458-92-4
Company Name: career henan chemical co
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Products Intro: Product Name:(DIFLUOROMETHOXY)BENZENE
CAS:458-92-4
Purity:98% Package:1KG;3USD
Company Name: Fuxin Pharmaceutical
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Products Intro: Product Name:Difluoromethoxybenzene
CAS:458-92-4
Purity:99% Package:1kg; 25kg; or larger package as required

(DIFLUOROMETHOXY)BENZENE manufacturers

(DIFLUOROMETHOXY)BENZENE Basic information
Product Name:(DIFLUOROMETHOXY)BENZENE
Synonyms:α,α-Difluoroanisole;A,A-DIFLUOROANISOLE;alpha-Difluoroanisole;(Difluoromethyl)phenyl ether;Difluoromethyl(phenyl) ether;Difluoromethylphenyl ether;Phenyl(difluoromethyl) ether;alpha,alpha-Difluoroanisole, Difluoromethyl phenyl ether
CAS:458-92-4
MF:C7H6F2O
MW:144.12
EINECS:207-283-1
Product Categories:
Mol File:458-92-4.mol
(DIFLUOROMETHOXY)BENZENE Structure
(DIFLUOROMETHOXY)BENZENE Chemical Properties
Boiling point 98 °C
density 1.2
refractive index 1.45
Fp 43.1±19.0℃
storage temp. Sealed in dry,Room Temperature
Specific Gravity1.200
AppearanceColorless to light yellow Liquid
λmax270nm(EtOH)(lit.)
CAS DataBase Reference458-92-4(CAS DataBase Reference)
Safety Information
Hazard Codes F
Risk Statements 10
Safety Statements 16-24/25-23
RIDADR 1993
HazardClass FLAMMABLE
PackingGroup III
HS Code 29093090
MSDS Information
(DIFLUOROMETHOXY)BENZENE Usage And Synthesis
Chemical PropertiesClear colorless liquid
Synthesis
Trifluoromethane

75-46-7

Phenol

108-95-2

(DIFLUOROMETHOXY)BENZENE

458-92-4

At room temperature, 0.28 g (0.003 mol) of phenol, 1.7 g (0.03 mol) of potassium hydroxide (KOH), an appropriate amount of water, and dioxane were added as solvents to a 50 mL round bottom flask. The reaction mixture was heated to 50°C, followed by the passage of trifluoromethane gas bubbling through the reaction solution for 2 hours. After completion of the reaction, the mixture was stirred at 50 °C overnight. The yield of difluoromethoxybenzene was calculated to be 70% by 19F NMR analysis (Figures 1 and 2 show the 19F NMR decoupling and proton coupling spectra of the reaction mixture and the purified difluoromethoxybenzene, respectively), using the 19F NMR integral signal of the HF2CO group as an internal standard.

References[1] Patent: WO2014/113412, 2014, A1. Location in patent: Page/Page column 4
[2] Journal of Organic Chemistry, 2013, vol. 78, # 17, p. 8904 - 8908
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