What is the 1-Bromo-2,4,6-trifluorobenzene?

1-Bromo-2,4,6-trifluorobenzene is clear colorless liquid, while it's Molecular Formula is C6H2BrF3. clear colorless liquid Used in Pharmaceutical Industry: 1-Bromo-2,4,6-trifluorobenzene is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block in the development of new drugs. Used in Chemical Synthesis: 1-Bromo-2,4,6-trifluorobenzene is used as a reactant in the Pd-catalyzed oxidative Heck reaction with allyl ester. This reaction is an important method for the formation of carbon-carbon bonds, which are crucial in the synthesis of complex organic molecules. Used in Material Science: Due to its packing polymorphism, 1-Bromo-2,4,6-trifluorobenzene can be utilized in the development of novel materials with unique properties. The ability to exist in different solid-state phases allows for the exploration of its potential applications in areas such as crystal engineering and material design. Used in Research and Development: 1-Bromo-2,4,6-trifluorobenzene serves as a valuable compound for research purposes, particularly in the fields of organic chemistry, medicinal chemistry, and materials science. Its unique properties and reactivity make it an interesting subject for further study and potential applications in various industries.

What is the CAS number for 1-Bromo-2,4,6-trifluorobenzene?

The CAS number of 1-Bromo-2,4,6-trifluorobenzene is 2367-76-2.

What is 1-Bromo-2,4,6-trifluorobenzene (2367-76-2) used for?

1-Bromo-2,4,6-trifluorobenzene is an organic compound that exhibits packing polymorphism in two nonidentical solid-state phases. It is a clear colorless liquid and is known to participate in Pd-catalyzed oxidative Heck reactions with allyl ester.InChI:InChI=1/C6H2Cl2F2/c7-4-1-3(9)2-5(8)6(4)10/h1-2H

What is the 1-Bromo-2,4,6-trifluorobenzene?

1-Bromo-2,4,6-trifluorobenzene is clear colorless liquid, while it's Molecular Formula is C6H2BrF3. clear colorless liquid Used in Pharmaceutical Industry: 1-Bromo-2,4,6-trifluorobenzene is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block in the development of new drugs. Used in Chemical Synthesis: 1-Bromo-2,4,6-trifluorobenzene is used as a reactant in the Pd-catalyzed oxidative Heck reaction with allyl ester. This reaction is an important method for the formation of carbon-carbon bonds, which are crucial in the synthesis of complex organic molecules. Used in Material Science: Due to its packing polymorphism, 1-Bromo-2,4,6-trifluorobenzene can be utilized in the development of novel materials with unique properties. The ability to exist in different solid-state phases allows for the exploration of its potential applications in areas such as crystal engineering and material design. Used in Research and Development: 1-Bromo-2,4,6-trifluorobenzene serves as a valuable compound for research purposes, particularly in the fields of organic chemistry, medicinal chemistry, and materials science. Its unique properties and reactivity make it an interesting subject for further study and potential applications in various industries.

What is the CAS number for 1-Bromo-2,4,6-trifluorobenzene?

The CAS number of 1-Bromo-2,4,6-trifluorobenzene is 2367-76-2.

What is 1-Bromo-2,4,6-trifluorobenzene (2367-76-2) used for?

1-Bromo-2,4,6-trifluorobenzene is an organic compound that exhibits packing polymorphism in two nonidentical solid-state phases. It is a clear colorless liquid and is known to participate in Pd-catalyzed oxidative Heck reactions with allyl ester.InChI:InChI=1/C6H2Cl2F2/c7-4-1-3(9)2-5(8)6(4)10/h1-2H

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1-Bromo-2,4,6-trifluorobenzene

CAS：2367-76-2
purity：99%

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Details

Factory Sells Best Quality 1-Bromo-2,4,6-trifluorobenzene 2367-76-2 with steady supply

Molecular Formula: C6H2BrF3
Molecular Weight: 210.981
Appearance/Colour: clear colorless liquid
Vapor Pressure: 1.7mmHg at 25°C
Melting Point: 3.5 °C(lit.)
Refractive Index: n20/D 1.485(lit.)
Boiling Point: 135.8 °C at 760 mmHg
Flash Point: 32.1 °C
PSA： 0.00000
Density: 1.784 g/cm³
LogP: 2.86640

1-Bromo-2,4,6-trifluorobenzene(Cas 2367-76-2) Usage

General Description

1-Bromo-2,4,6-trifluorobenzene exhibits packing polymorphism in two nonidentical solid-state phases. 1-Bromo-2,4,6-trifluorobenzene participates in Pd-catalyzed oxidative Heck reaction with allyl ester.

InChI:InChI=1/C6H2Cl2F2/c7-4-1-3(9)2-5(8)6(4)10/h1-2H

2367-76-2 Relevant articles

PROCESS FOR PREPARATION OF HALO SUBSTITUTED BENZOIC ACID COMPOUND AND INTERMEDIATES THEREOF

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Page/Page column 13, (2018/09/28)

The present invention provides a process...

A new Knoevenagel-type synthesis of fully substituted γ- hydroxybutenolides

Lamberth, Clemens,Godineau, Edouard,Smejkal, Tomas,Trah, Stephan

scheme or table, p. 4117 - 4120 (2012/08/29)

The synthesis of fully substituted γ-hyd...

Method for the production of substituted 2-aryl malonic acid esters

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Page/Page column 4, (2010/04/23)

The present invention relates to a proce...

Gold-catalyzed halogenation of aromatics by N-halosuccinimides

Mo, Fanyang,Yan, Jerry Mingtao,Qiu, Di,Li, Fei,Zhang, Yan,Wang, Jianbo

scheme or table, p. 2028 - 2032 (2010/06/17)

(Chemical Equation Presented) Golden bro...

2367-76-2 Process route

: 2265-94-3
1,3-difluoro-5-nitrobenzene

: 2367-76-2
2,4,6-trifluorobromobenzene

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: iron; aqueous NH₄Cl 3: iron; bromine With bromine; iron; ammonium chloride;
Multi-step reaction with 3 steps 1: iron; aqueous NH₄Cl 3: iron; bromine With bromine; iron; ammonium chloride;
Multi-step reaction with 3 steps 1: iron; aqueous NH₄Cl 3: iron; bromine With bromine; iron; ammonium chloride;
Multi-step reaction with 3 steps 1: iron; aqueous NH₄Cl 3: iron; bromine With bromine; iron; ammonium chloride;

: 364-30-7
2-amino-3,5-difluoronitrobenzene

: 2367-76-2
2,4,6-trifluorobromobenzene

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: sulfuric acid; aqueous phosphoric acid; nitrosylsulfuric acid / anschliessendes Behandeln mit Natriumhypophosphit-Loesung und Kupfer(I)-oxid 2: iron; aqueous NH₄Cl 4: iron; bromine With nitrosylsulfuric acid; phosphoric acid; sulfuric acid; bromine; iron; ammonium chloride;
Multi-step reaction with 4 steps 1: sulfuric acid; aqueous phosphoric acid; nitrosylsulfuric acid / anschliessendes Behandeln mit Natriumhypophosphit-Loesung und Kupfer(I)-oxid 2: iron; aqueous NH₄Cl 4: iron; bromine With nitrosylsulfuric acid; phosphoric acid; sulfuric acid; bromine; iron; ammonium chloride;
Multi-step reaction with 4 steps 1: sulfuric acid; aqueous phosphoric acid; nitrosylsulfuric acid / anschliessendes Behandeln mit Natriumhypophosphit-Loesung und Kupfer(I)-oxid 2: iron; aqueous NH₄Cl 4: iron; bromine With nitrosylsulfuric acid; phosphoric acid; sulfuric acid; bromine; iron; ammonium chloride;
Multi-step reaction with 4 steps 1: sulfuric acid; aqueous phosphoric acid; nitrosylsulfuric acid / anschliessendes Behandeln mit Natriumhypophosphit-Loesung und Kupfer(I)-oxid 2: iron; aqueous NH₄Cl 4: iron; bromine With nitrosylsulfuric acid; phosphoric acid; sulfuric acid; bromine; iron; ammonium chloride;