What is the 4-Fluorobenzotrifluoride?

4-Fluorobenzotrifluoride is Clear colourless to light yellow liquid, while it's Molecular Formula is C7H4F4. Clear colourless to light yellow liquid 4-Fluorobenzotrifluoride was used in the synthesis of 2,2?-bis(trifluoromethylphenoxy)biphenyl via nucleophilic aromatic substitution reaction with 2,2?-biphenol, (S)-fluoxetine, potent inhibitor of neuronal serotonin-uptake and 1-aryloxy-2-substituted aminomethyltetrahydronaphthalene derivatives.

What is the CAS number for 4-Fluorobenzotrifluoride?

The CAS number of 4-Fluorobenzotrifluoride is 402-44-8.

What is 4-Fluorobenzotrifluoride (402-44-8) used for?

4-Fluorobenzotrifluoride, also known as α,α,α-trifluorotoluene, is an aromatic compound belonging to the family of fluorinated aromatics. It is characterized by the presence of a fluorine atom at the para position and three fluorine atoms on the benzene ring, which imparts unique chemical and physical properties to the molecule. As a clear, colorless to light yellow liquid, 4-Fluorobenzotrifluoride is known for its reactivity in various chemical reactions, making it a versatile building block in the synthesis of a wide range of organic compounds.InChI:InChI=1/C7H4F4/c8-6-3-1-5(2-4-6)7(9,10)11/h1-4H

What is the 4-Fluorobenzotrifluoride?

4-Fluorobenzotrifluoride is Clear colourless to light yellow liquid, while it's Molecular Formula is C7H4F4. Clear colourless to light yellow liquid 4-Fluorobenzotrifluoride was used in the synthesis of 2,2?-bis(trifluoromethylphenoxy)biphenyl via nucleophilic aromatic substitution reaction with 2,2?-biphenol, (S)-fluoxetine, potent inhibitor of neuronal serotonin-uptake and 1-aryloxy-2-substituted aminomethyltetrahydronaphthalene derivatives.

What is the CAS number for 4-Fluorobenzotrifluoride?

The CAS number of 4-Fluorobenzotrifluoride is 402-44-8.

What is 4-Fluorobenzotrifluoride (402-44-8) used for?

4-Fluorobenzotrifluoride, also known as α,α,α-trifluorotoluene, is an aromatic compound belonging to the family of fluorinated aromatics. It is characterized by the presence of a fluorine atom at the para position and three fluorine atoms on the benzene ring, which imparts unique chemical and physical properties to the molecule. As a clear, colorless to light yellow liquid, 4-Fluorobenzotrifluoride is known for its reactivity in various chemical reactions, making it a versatile building block in the synthesis of a wide range of organic compounds.InChI:InChI=1/C7H4F4/c8-6-3-1-5(2-4-6)7(9,10)11/h1-4H

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402-44-8

Product Name：4-Fluorobenzotrifluoride
Molecular Formula：C₇H₄F₄
Purity：99%
Molecular Weight：164.102

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Product Details;

CasNo： 402-44-8

Molecular Formula： C₇H₄F₄

Appearance： Clear colourless to light yellow liquid

factory and supplier 402-44-8 4-Fluorobenzotrifluoride in stock

Molecular Formula:C7H4F4
Molecular Weight:164.102
Appearance/Colour:Clear colourless to light yellow liquid
Vapor Pressure:35.8mmHg at 25°C
Melting Point:-42--41.7 °C(lit.)
Refractive Index:n20/D 1.401(lit.)
Boiling Point:104.5 °C at 760 mmHg
Flash Point:10.6 °C
PSA：0.00000
Density:1.29 g/cm³
LogP:2.84450

4-Fluorobenzotrifluoride(Cas 402-44-8) Usage

Synthesis Reference(s)

Tetrahedron, 49, p. 8129, 1993 DOI: 10.1016/S0040-4020(01)88032-7

InChI:InChI=1/C7H4F4/c8-6-3-1-5(2-4-6)7(9,10)11/h1-4H

402-44-8 Relevant articles

Cross-Coupling through Ag(I)/Ag(III) Redox Manifold

Demonti, Luca,Mézailles, Nicolas,Nebra, Noel,Saffon-Merceron, Nathalie

supporting information, p. 15396 - 15405 (2021/10/12)

In ample variety of transformations, the...

Fluorination of arylboronic esters enabled by bismuth redox catalysis

Planas, Oriol,Wang, Feng,Leutzsch, Markus,Cornella, Josep

, p. 313 - 317 (2020/01/28)

Bismuth catalysis has traditionally reli...

Oxidatively Induced Aryl-CF3 Coupling at Diphosphine Nickel Complexes

Bour, James R.,Roy, Pronay,Canty, Allan J.,Kampf, Jeff W.,Sanford, Melanie S.

supporting information, p. 3 - 7 (2020/01/03)

This communication describes the synthes...

Mechanism of Photoredox-Initiated C-C and C-N Bond Formation by Arylation of IPrAu(I)-CF3 and IPrAu(I)-Succinimide

Kim, Suhong,Toste, F. Dean

, p. 4308 - 4315 (2019/01/25)

Herein, we report on the photoredox-init...

402-44-8 Process route

: C₄₁H₃₂F₄FeNiP₂

: lithium chloride

: 67292-34-6
[1,1'-bis(diphenylphosphino)ferrocene]nickel(II) chloride

: 402-44-8
4-Fluorobenzotrifluoride

Conditions

Conditions	Yield
With ferrocenium hexafluorophosphate; In acetone; at 23 ℃; for 0.5h; Inert atmosphere; Glovebox;	72 %Spectr.

: C₃₃H₂₈F₄NiP₂

: 456-22-4
4-Fluorobenzoic acid

: 402-44-8
4-Fluorobenzotrifluoride

Conditions

Conditions	Yield
With ferrocenium hexafluorophosphate; water; In acetone; at 25 ℃; for 0.5h; Inert atmosphere; Glovebox;	65 %Spectr. 18 %Spectr.

402-44-8 Upstream products

402-42-6
4-fluoro-1-trichloromethylbenzene
56-23-5
tetrachloromethane
462-06-6
fluorobenzene
455-14-1
4-trifluoromethylphenylamine

402-44-8 Downstream products

367-86-2
1-fluoro-2-nitro-4-trifluoromethyl-benzene
115029-23-7
2-fluoro-5-(trifluoromethyl)benzoic acid
125923-59-3
methyl difluoro(4-fluorophenyl)acetate
128470-60-0
Benzyl-methyl-[1-(4-trifluoromethyl-phenoxy)-indan-2-ylmethyl]-amine