What is the Benzotrifluoride?

Benzotrifluoride is Clear colourless to light yellow liquid, while it's Molecular Formula is C7H5F3. Clear colourless to light yellow liquid It is applied as an alternative solvent to dichloromethane, where it has a higher bp. It is used as an intermediate for dyes and pharmaceuticals, as a solvent and a dielectric fluid, a vulcanizing agent.

What is the CAS number for Benzotrifluoride?

The CAS number of Benzotrifluoride is 98-08-8.

What is Benzotrifluoride (98-08-8) used for?

Benzotrifluoride, also known as (trifluoromethyl)benzene, is a fluorohydrocarbon that is fluoroform in which the hydrogen is substituted by a phenyl group. It is a colorless to light yellow liquid with an aromatic odor, low viscosity, and intermediate polarity between dichloromethane and ethyl acetate. Benzotrifluoride is miscible with common organic solvents and can dissolve many organic compounds. It has a role as a solvent and an environmental contaminant and is a member of (trifluoromethyl)benzenes.InChI:InChI=1/C7H5F3/c8-7(9,10)6-4-2-1-3-5-6/h1-5H

What is the Benzotrifluoride?

Benzotrifluoride is Clear colourless to light yellow liquid, while it's Molecular Formula is C7H5F3. Clear colourless to light yellow liquid It is applied as an alternative solvent to dichloromethane, where it has a higher bp. It is used as an intermediate for dyes and pharmaceuticals, as a solvent and a dielectric fluid, a vulcanizing agent.

What is the CAS number for Benzotrifluoride?

The CAS number of Benzotrifluoride is 98-08-8.

What is Benzotrifluoride (98-08-8) used for?

Benzotrifluoride, also known as (trifluoromethyl)benzene, is a fluorohydrocarbon that is fluoroform in which the hydrogen is substituted by a phenyl group. It is a colorless to light yellow liquid with an aromatic odor, low viscosity, and intermediate polarity between dichloromethane and ethyl acetate. Benzotrifluoride is miscible with common organic solvents and can dissolve many organic compounds. It has a role as a solvent and an environmental contaminant and is a member of (trifluoromethyl)benzenes.InChI:InChI=1/C7H5F3/c8-7(9,10)6-4-2-1-3-5-6/h1-5H

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98-08-8

Product Name：Benzotrifluoride
Molecular Formula：C₇H₅F₃
Purity：99%
Molecular Weight：146.112

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Product Details;

CasNo： 98-08-8

Molecular Formula： C₇H₅F₃

Appearance： Clear colourless to light yellow liquid

factory and supplier 98-08-8 Benzotrifluoride in stock

Molecular Formula:C7H5F3
Molecular Weight:146.112
Appearance/Colour:Clear colourless to light yellow liquid
Vapor Pressure:35.3mmHg at 25°C
Melting Point:-29 °C(lit.)
Refractive Index:1.414
Boiling Point:104.769 °C at 760 mmHg
Flash Point:12.222 °C
PSA：0.00000
Density:1.188 1.118 g/cm^>3
LogP:2.70540

Benzotrifluoride(Cas 98-08-8) Usage

Air & Water Reactions	Highly flammable. Insoluble in water.
Reactivity Profile	Benzotrifluoride may react with oxidizing materials, strong bases and reducing agents.
Hazard	Highly toxic by inhalation. Flammable, dangerous fire risk.
Fire Hazard	HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
Flammability and Explosibility	Notclassified
Safety Profile	Poison by intraperitoneal route.Moderately toxic by subcutaneous route. Dangerous fire hazard. To fight fire, usewater, foam, CO2, spray mist, dry chemical. When heatedto decomposition it emits toxic fumes of F??. Incompatiblewith oxidizing materials
Purification Methods	Purify benzotrifluoride by repeated treatment with boiling aqueous Na2CO3 (until no test for chloride ion is obtained), dry it with K2CO3, then with P2O5, and fractionally distil it. [Beilstein 5 IV 802.]
Definition	ChEBI: (trifluoromethyl)benzene is a fluorohydrocarbon that is fluoroform in which the hydrogen is substituted by a phenyl group. It has a role as a solvent and an environmental contaminant. It is a fluorohydrocarbon and a member of (trifluoromethyl)benzenes. It derives from a fluoroform.
General Description	A clear colorless liquid with an aromatic odor. Flash point of 54°F. Vapors are heavier than air. Insoluble in water and slightly denser than water. May be toxic by inhalation.

InChI:InChI=1/C7H5F3/c8-7(9,10)6-4-2-1-3-5-6/h1-5H

98-08-8 Relevant articles

A NEW METHOD FOR THE TRIFLUOROMETHYLATION OF AROMATIC COMPOUNDS

Marhold, A.,Klauke, E.

, p. 516 (1980)

Trifluoromethylation of organic halides with methyl halodifluoroacetates - a process via difluorocarbene and trifluoromethide intermediates

Duan, Jian-Xing,Su, De-Bao,Chen, Qing-Yun

, p. 279 - 284 (1993)

Treatment of methyl halodifluoroacetates...

Aryl-CF3 Coupling from Phosphinoferrocene-Ligated Palladium(II) Complexes

Ferguson, Devin M.,Bour, James R.,Canty, Allan J.,Kampf, Jeff W.,Sanford, Melanie S.

, p. 519 - 526 (2019)

This article describes a detailed invest...

New Vistas in Transmetalation with Discrete “AgCF3” Species: Implications in Pd-Mediated Trifluoromethylation Reactions

Martínez de Salinas, Sara,Mudarra, ángel L.,Benet-Buchholz, Jordi,Parella, Teodor,Maseras, Feliu,Pérez-Temprano, Mónica H.

, p. 11895 - 11898 (2018)

This work describes the employment of di...

Application of Visible-to-UV Photon Upconversion to Photoredox Catalysis: The Activation of Aryl Bromides

Majek, Michal,Faltermeier, Uwe,Dick, Bernhard,Pérez-Ruiz, Raúl,JacobivonWangelin, Axel

, p. 15496 - 15501 (2015)

The activation of aryl-Br bonds was achi...

Photoredox-catalyzed reduction of halogenated arenes in water by amphiphilic polymeric nanoparticles

Eisenreich, Fabian,Kuster, Tom H. R.,Palmans, Anja R. A.,van Krimpen, David

supporting information, (2021/10/05)

The use of organic photoredox catalysts ...

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...

Mechanistic Insight into Copper-Mediated Trifluoromethylation of Aryl Halides: The Role of CuI

Jin, Yuxuan,Leng, Xuebing,Liu, He,Shen, Qilong,Wu, Jian

, p. 14367 - 14378 (2021/09/13)

The synthesis, characterization, and rea...

H2-Free Selective Dehydroxymethylation of Primary Alcohols over Palladium Nanoparticle Catalysts

Yamaguchi, Sho,Kondo, Hiroki,Uesugi, Kohei,Sakoda, Katsumasa,Jitsukawa, Koichiro,Mitsudome, Takato,Mizugaki, Tomoo

, p. 1135 - 1139 (2020/12/29)

The dehydroxymethylation of primary alco...

98-08-8 Process route

: 55642-42-7
bis(trifluoromethyl)tellurium

: 108-90-7
chlorobenzene

: 75-46-7
trifluoromethan

: 1718-20-3
bis(trifluoromethyl) ditelluride

: 98-08-8
α,α,α-trifluorotoluene

: 98-56-6
4-chlorobenzotrifluoride

: 98-15-7
3-chlorotrifluoromethylbenzene

: 88-16-4
1-chloro-2-(trifluoromethyl)benzene

Conditions

Conditions	Yield
at 168 ℃; for 120h; Product distribution;

: 98-07-7
Benzotrichlorid

: 98-08-8
α,α,α-trifluorotoluene

: 498-67-9
(dichlorofluoromethyl)benzene

: 349-50-8
(chlorodifluoromethyl)benzene