352-32-9

  • Product Name:4-Fluorotoluene
  • Molecular Formula:C7H7F
  • Purity:99%
  • Molecular Weight:110.131
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Product Details;

CasNo: 352-32-9

Molecular Formula: C7H7F

Appearance: clear colorless to slightly yellow liquid

factory and supplier 352-32-9 4-Fluorotoluene in stock

  • Molecular Formula:C7H7F
  • Molecular Weight:110.131
  • Appearance/Colour:clear colorless to slightly yellow liquid 
  • Vapor Pressure:21.1mmHg at 25°C 
  • Melting Point:-56 °C 
  • Refractive Index:n20/D 1.468(lit.)  
  • Boiling Point:117 °C at 760 mmHg 
  • Flash Point:11.9 °C 
  • PSA:0.00000 
  • Density:1.001 g/cm3 
  • LogP:2.13410 

p-Fluorotoluene(Cas 352-32-9) Usage

Air & Water Reactions

Highly flammable.

Reactivity Profile

p-Fluorotoluene may be incompatible with strong oxidizing and reducing agents. May be incompatible with amines, nitrides, azo/diazo compounds, alkali metals, and epoxides. Products of combustion contain toxic fluoride fumes.

Fire Hazard

Special Hazards of Combustion Products: Toxic fumes of fluoride

Safety Profile

Moderately toxic by parenteral route. A very dangerous fire hazard when exposed to heat or flame; can react vigorously with oxibzing materials. When heated to decomposition it emits toxic fumes of F-. See also FLUORIDES.

Purification Methods

Purify it as for o-fluorotoluene. [Beilstein 5 H 290, 5 III 677, 5 IV 799.]

General Description

A colorless liquid with an aromatic odor. May float or sink in water.

InChI:InChI=1/C7H7F/c1-6-2-4-7(8)5-3-6/h2-5H,1H3

352-32-9 Relevant articles

Liquid-phase fluorination of aromatic compounds by elemental fluorine

Conte, L.,Gambaretto, G. P.,Napoli, M.,Fraccaro, C.,Legnaro, E.

, p. 175 - 180 (1995)

The fluorination of aromatic compounds (...

Direct fluorination of toluene using elemental fluorine in gas/liquid microreactors

J?hnisch,Baerns,Hessel,Ehrfeld,Haverkamp,L?we,Wille,Guber

, p. 117 - 128 (2000)

Direct fluorination of toluene, pure or ...

Gas-phase alkylation of fluorobenzene and substituted fluorobenzene by (CH3)2F+ ions

Attina,Ricci

, p. 6775 - 6778 (1991)

The gas-phase methylation of selected fl...

Exhaustive chlorination of [B12H12]2- without chlorine gas and the use of [B12Cl12]2- as a supporting anion in catalytic hydrodefluorination of aliphatic C-F bonds

Gu, Weixing,Ozerov, Oleg V.

, p. 2726 - 2728 (2011)

The fully chlorinated closo-dodecaborate...

Full continuous flow synthesis process of fluorine-containing aromatic hydrocarbon compounds

-

Paragraph 0081-0094, (2021/04/07)

The invention provides a full continuous...

A Mild, General, Metal-Free Method for Desulfurization of Thiols and Disulfides Induced by Visible-Light

Qiu, Wenting,Shi, Shuai,Li, Ruining,Lin, Xianfeng,Rao, Liangming,Sun, Zhankui

supporting information, p. 1255 - 1258 (2021/05/05)

A visible-light-induced metal-free desul...

Coupling Photocatalysis and Substitution Chemistry to Expand and Normalize Redox-Active Halides

Rathnayake, Manjula D.,Weaver, Jimmie D.

supporting information, p. 2036 - 2041 (2021/04/05)

Photocatalysis can generate radicals in ...

Hydrodehalogenation of organohalides by Et3SiH catalysed by group 4 metal complexes and B(C6F5)3

?ilková, Nadě?da,Dunlop, David,Horá?ek, Michal,Lama?, Martin,Pinkas, Ji?í

supporting information, p. 2771 - 2775 (2020/03/13)

Catalytic hydrodehalogenation (HDH) of a...

352-32-9 Process route

o-tolyl(p-tolyl)iodonium trifluoromethanesulfonate

o-tolyl(p-tolyl)iodonium trifluoromethanesulfonate

p-fluorotoluene
352-32-9

p-fluorotoluene

ortho-methylphenyl iodide
615-37-2

ortho-methylphenyl iodide

2-Fluorotoluene
95-52-3

2-Fluorotoluene

4-tolyl iodide
624-31-7

4-tolyl iodide

toluene
108-88-3,15644-74-3,16713-13-6

toluene

Conditions
Conditions Yield
With cesium fluoride; In acetonitrile; at 85 ℃; for 0.666667h; GC-MS estimated relative yields;
4-methylphenyliodonium-(5-[2,2-dimethyl-1,3-dioxane-4,6-dione])ylide
1250409-78-9

4-methylphenyliodonium-(5-[2,2-dimethyl-1,3-dioxane-4,6-dione])ylide

p-fluorotoluene
352-32-9

p-fluorotoluene

4-tolyl iodide
624-31-7

4-tolyl iodide

toluene
108-88-3,15644-74-3,16713-13-6

toluene

Conditions
Conditions Yield
With potassium fluoride; [2.2.2]cryptande; In N,N-dimethyl-formamide; at 130 ℃; for 0.25h; Reactivity; sealed tube;

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