What is the (Trifluoromethoxy)benzene?

(Trifluoromethoxy)benzene is Colorless to light yellow liquid, while it's Molecular Formula is C7H5F3O. Colorless to light yellow liquid Used in Pharmaceutical Industry: (Trifluoromethoxy)benzene is used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly those with potential applications in treating a range of diseases. Its unique trifluoromethyl ether group allows for the development of novel drug candidates with improved pharmacokinetic and pharmacodynamic properties. Used in Agrochemical Industry: In the agrochemical sector, (trifluoromethoxy)benzene serves as a crucial building block for the creation of new pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness, selectivity, and environmental compatibility. Used in Material Science: (Trifluoromethoxy)benzene is utilized in the development of advanced materials, such as polymers and coatings, that exhibit improved properties like chemical resistance, thermal stability, and non-stick characteristics. Its presence in these materials can lead to innovative applications in various industries, including automotive, aerospace, and electronics. Used in Fine Chemicals Synthesis: As a versatile intermediate, (Trifluoromethoxy)benzene is employed in the synthesis of fine chemicals, including fragrances, dyes, and specialty chemicals. Its unique structure and reactivity enable the production of high-value compounds with specific applications in various markets.

What is the CAS number for (Trifluoromethoxy)benzene?

The CAS number of (Trifluoromethoxy)benzene is 456-55-3.

What is (Trifluoromethoxy)benzene (456-55-3) used for?

(Trifluoromethoxy)benzene, an aryl trifluoromethyl ether, is a colorless to light yellow liquid with unique chemical properties. It can be synthesized from 4-chloro-1-(trifluoromethoxy)benzene through hydrogenolysis, and its conformation in the gas phase has been studied using electron diffraction, spectroscopy, and ab initio calculations.InChI:InChI=1/C7H5F3O/c8-7(9,10)11-6-4-2-1-3-5-6/h1-5H

What is the (Trifluoromethoxy)benzene?

(Trifluoromethoxy)benzene is Colorless to light yellow liquid, while it's Molecular Formula is C7H5F3O. Colorless to light yellow liquid Used in Pharmaceutical Industry: (Trifluoromethoxy)benzene is used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly those with potential applications in treating a range of diseases. Its unique trifluoromethyl ether group allows for the development of novel drug candidates with improved pharmacokinetic and pharmacodynamic properties. Used in Agrochemical Industry: In the agrochemical sector, (trifluoromethoxy)benzene serves as a crucial building block for the creation of new pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness, selectivity, and environmental compatibility. Used in Material Science: (Trifluoromethoxy)benzene is utilized in the development of advanced materials, such as polymers and coatings, that exhibit improved properties like chemical resistance, thermal stability, and non-stick characteristics. Its presence in these materials can lead to innovative applications in various industries, including automotive, aerospace, and electronics. Used in Fine Chemicals Synthesis: As a versatile intermediate, (Trifluoromethoxy)benzene is employed in the synthesis of fine chemicals, including fragrances, dyes, and specialty chemicals. Its unique structure and reactivity enable the production of high-value compounds with specific applications in various markets.

What is the CAS number for (Trifluoromethoxy)benzene?

The CAS number of (Trifluoromethoxy)benzene is 456-55-3.

What is (Trifluoromethoxy)benzene (456-55-3) used for?

(Trifluoromethoxy)benzene, an aryl trifluoromethyl ether, is a colorless to light yellow liquid with unique chemical properties. It can be synthesized from 4-chloro-1-(trifluoromethoxy)benzene through hydrogenolysis, and its conformation in the gas phase has been studied using electron diffraction, spectroscopy, and ab initio calculations.InChI:InChI=1/C7H5F3O/c8-7(9,10)11-6-4-2-1-3-5-6/h1-5H

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456-55-3

Product Name：Trifluoromethoxybenzene
Molecular Formula：C₇H₅F₃O
Purity：99%
Molecular Weight：162.111

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Product Details;

CasNo： 456-55-3

Molecular Formula： C₇H₅F₃O

Appearance： Colorless to light yellow liquid

factory and supplier 456-55-3 Trifluoromethoxybenzene in stock

Molecular Formula:C7H5F3O
Molecular Weight:162.111
Appearance/Colour:Colorless to light yellow liquid
Vapor Pressure:41.3 mm Hg ( 25 °C)
Melting Point:-50oC
Refractive Index:n20/D 1.406(lit.)
Boiling Point:102.8 °C at 760 mmHg
Flash Point:12.2 °C
PSA：9.23000
Density:1.248 g/cm³
LogP:2.58520

(Trifluoromethoxy)benzene(Cas 456-55-3) Usage

Synthesis Reference(s)	The Journal of Organic Chemistry, 29, p. 1, 1964 DOI: 10.1021/jo01024a001
General Description	(Trifluoromethoxy)benzene is an aryl trifluoromethyl ether. (Trifluoromethoxy)benzene can be prepared from 4-chloro-1-(trifluoromethoxy)benzene via hydrogenolysis. Conformation of (trifluoromethoxy)benzene in the gas phase has been studied by electron diffraction and spectroscopy supplemented with ab initio calculations.

InChI:InChI=1/C7H5F3O/c8-7(9,10)11-6-4-2-1-3-5-6/h1-5H

456-55-3 Relevant articles

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Allison,Cady

, p. 1089 (1959)

Synthesis conditions and activity of various Lewis acids for the fluorination of trichloromethoxy-benzene by HF in liquid phase

Salomé,Mauger,Brunet,Schanen

, p. 1947 - 1950 (2004)

The experimental conditions (temperature...

Radical Hydrodehalogenation of Aryl Halides with H2 Catalyzed by a Phenanthroline-Based PNNP Cobalt(I) Complex

Iizuka, Kosuke,Ishizaka, Yusuke,Jheng, Nai-Yuan,Minami, Yasunori,Naganawa, Yuki,Nakajima, Yumiko,Sekiguchi, Akira

, p. 2320 - 2329 (2022/02/16)

Radical hydrodehalogenation of aryl hali...

Radical C?H Trifluoromethoxylation of (Hetero)arenes with Bis(trifluoromethyl)peroxide

Dix, Stefan,Golz, Paul,Schmid, Jonas R.,Riedel, Sebastian,Hopkinson, Matthew N.

supporting information, p. 11554 - 11558 (2021/07/09)

Trifluoromethoxylated (hetero)arenes are...

Direct Trifluoromethylation of Alcohols Using a Hypervalent Iodosulfoximine Reagent

Kalim, Jorna,Duhail, Thibaut,Pietrasiak, Ewa,Anselmi, Elsa,Magnier, Emmanuel,Togni, Antonio

supporting information, p. 2638 - 2642 (2021/01/21)

The direct trifluoromethylation of a var...

Electrochemical Activation of Diverse Conventional Photoredox Catalysts Induces Potent Photoreductant Activity**

Chernowsky, Colleen P.,Chmiel, Alyah F.,Wickens, Zachary K.

, p. 21418 - 21425 (2021/08/25)

Herein, we disclose that electrochemical...

456-55-3 Process route

: 71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1
benzene

: 426-58-4
(trifluoromethylsulfonyl)benzene

: 456-55-3
1-trifluoromethoxybenzene

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: boron trifluoride boron trifluoride;

: 456-56-4
phenyl trifluoromethylsulfide

: 426-58-4
(trifluoromethylsulfonyl)benzene

: 456-55-3
1-trifluoromethoxybenzene