443-88-9

  • Product Name:2,6-Dimethylfluorobenzene
  • Molecular Formula:C8H9F
  • Purity:99%
  • Molecular Weight:124.158
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Product Details;

CasNo: 443-88-9

Molecular Formula: C8H9F

factory and supplier 443-88-9 2,6-Dimethylfluorobenzene in stock

  • Molecular Formula:C8H9F
  • Molecular Weight:124.158
  • Vapor Pressure:6.56mmHg at 25°C 
  • Refractive Index:n20/D 1.479(lit.)  
  • Boiling Point:143.9 °C at 760 mmHg 
  • Flash Point:30.4 °C 
  • PSA:0.00000 
  • Density:0.983 g/cm3 
  • LogP:2.44250 

2,6-Dimethylfluorobenzene(Cas 443-88-9) Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 21, p. 906, 1978 DOI: 10.1021/jm00207a013

InChI:InChI=1/C8H9F/c1-6-4-3-5-7(2)8(6)9/h3-5H,1-2H3

443-88-9 Relevant articles

Azoacetylenes for the Synthesis of Arylazotriazole Photoswitches

Anderl, Felix,Balkenhohl, Moritz,Carreira, Erick M.,Fink, Moritz,Pfaff, Patrick

, p. 14495 - 14501 (2021/09/18)

We report a modular approach toward nove...

Expanding the Balz–Schiemann Reaction: Organotrifluoroborates Serve as Competent Sources of Fluoride Ion for Fluoro-Dediazoniation

Mohy El Dine, Tharwat,Sadek, Omar,Gras, Emmanuel,Perrin, David M.

supporting information, p. 14933 - 14937 (2018/09/25)

The Balz–Schiemann reaction endures as a...

Fluorination of aryl boronic acids using acetyl hypofluorite made directly from diluted fluorine

Vints, Inna,Gatenyo, Julia,Rozen, Shlomo

, p. 11794 - 11797 (2014/01/06)

Aryl boronic acids or pinacol esters con...

Cu-catalyzed fluorination of diaryliodonium salts with KF

Ichiishi, Naoko,Canty, Allan J.,Yates, Brian F.,Sanford, Melanie S.

supporting information, p. 5134 - 5137 (2013/10/22)

A mild Cu-catalyzed nucleophilic fluorin...

443-88-9 Process route

2,6-dimethylaniline
87-62-7

2,6-dimethylaniline

2-fluoro-m-xylene
443-88-9

2-fluoro-m-xylene

Conditions
Conditions Yield
With sodium nitrite; In Et3N-3HF; diethyl ether;
86.3%
With hydrogenchloride; sodium tetrafluoroborate; sodium nitrite; In water; at 0 - 5 ℃;
41%
Multistep reaction; (i) NaNO2, aq. HBF4, THF, (ii) benzene;
Multi-step reaction with 2 steps
1: 60 percent / 37percent aq.HCl, NaNO2, HBF4 / 0.5 h / 1.) 10 deg C, 2.) 0 - 10 deg C, 10 min.
2: 53 percent / 0.5 h / Heating
With hydrogenchloride; tetrafluoroboric acid; sodium nitrite;
2,6-dimethylaniline; With phosphoric acid; In tert-butyl alcohol; Inert atmosphere;
With tert.-butylnitrite; potassium phenyltrifluoborate; In tert-butyl alcohol; at 20 - 50 ℃; for 2.33333h; Inert atmosphere;
With 2,4-Dinitrofluorobenzene; In dimethylsulfoxide-d6; tert-butyl alcohol; at 20 ℃; Inert atmosphere;
50 %Spectr.
Multi-step reaction with 2 steps
1: ethyl acetate / 0 °C / Inert atmosphere
2: [D3]acetonitrile
In [D3]acetonitrile; ethyl acetate;
2,6-dimethylphenyl chloroformic acid ester
876-99-3

2,6-dimethylphenyl chloroformic acid ester

2-fluoro-m-xylene
443-88-9

2-fluoro-m-xylene

Conditions
Conditions Yield
With hydrogen fluoride; In various solvent(s); at 140 ℃; for 6h; under 19501.6 Torr;
90%
Multi-step reaction with 2 steps
1: 80 percent / potassium fluoride, 18-crown-6 / CH2Cl2 / 5 h / other reagent: hydrogen fluoride
2: 40 percent / SbF5 / 180 h / Heating
With potassium fluoride; 18-crown-6 ether; antimony pentafluoride; In dichloromethane;

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