1072-85-1

  • Product Name:2-Bromofluorobenzene
  • Molecular Formula:C6H4BrF
  • Purity:99%
  • Molecular Weight:175
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Product Details;

CasNo: 1072-85-1

Molecular Formula: C6H4BrF

Appearance: clear colourless to light yellow liquid

factory and supplier 1072-85-1 2-Bromofluorobenzene in stock

  • Molecular Formula:C6H4BrF
  • Molecular Weight:175
  • Appearance/Colour:clear colourless to light yellow liquid 
  • Vapor Pressure:4.67mmHg at 25°C 
  • Melting Point:-8°C 
  • Refractive Index:n20/D 1.534(lit.)  
  • Boiling Point:151.5 °C at 760 mmHg 
  • Flash Point:50.2 °C 
  • PSA:0.00000 
  • Density:1.593 g/cm3 
  • LogP:2.58820 

2-Bromofluorobenzene(Cas 1072-85-1) Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 26, p. 5149, 1961 DOI: 10.1021/jo01070a089

InChI:InChI=1/C6H4BrF/c7-5-3-1-2-4-6(5)8/h1-4H

1072-85-1 Relevant articles

Exchange of halogens between aromatic compounds in the presence of Cu-HZSM-5 zeolite

Imhaoulne,Imhaoulene,Vivier,Guisnet,Petot,Perot,Gubelmann

, p. 12913 - 12922 (1994)

The reactions between various haloaromat...

Reactions of aromatic compounds with xenon difluoride

Bardin,Adonin, N. Yu.

, p. 1400 - 1407 (2016)

Reactions of substituted benzenes C6H5R ...

Hydroxyl radical induced reactions with 1-bromo-2-fluorobenzene in aqueous solutions: Formation of radical cations

Mohan, Hari,Mittal, Jai P.

, p. 263 - 270 (1996)

Hydroxyl radicals are observed to react ...

-

Simmons,H.E.

, p. 1657 - 1664 (1961)

-

Substrate Selectivity and Orientation in Aromatic Substitution by Molecular Fluorine

Cacace, F.,Giacomello, P.,Wolf, A. P.

, p. 3511 - 3515 (1980)

Direct elemental fluorination of represe...

Radical Decarboxylative Carbometalation of Benzoic Acids: A Solution to Aromatic Decarboxylative Fluorination

Xu, Peng,López-Rojas, Priscila,Ritter, Tobias

, p. 5349 - 5354 (2021)

Abundant aromatic carboxylic acids exist...

Fluorination of arylboronic esters enabled by bismuth redox catalysis

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

, p. 313 - 317 (2020)

Bismuth catalysis has traditionally reli...

Palladium-catalysed electrophilic aromatic C-H fluorination

Yamamoto, Kumiko,Li, Jiakun,Garber, Jeffrey A. O.,Rolfes, Julian D.,Boursalian, Gregory B.,Borghs, Jannik C.,Genicot, Christophe,Jacq, Jér?me,Van Gastel, Maurice,Neese, Frank,Ritter, Tobias

, p. 511 - 514 (2018/03/02)

Aryl fluorides are widely used in the ph...

DIRECT PALLADIUM-CATALYZED AROMATIC FLUORINATION

-

Paragraph 00186; 00187, (2017/09/27)

Provided herein are palladium complexes ...

1072-85-1 Process route

bromobenzene
108-86-1,52753-63-6

bromobenzene

o-fluorobromobenzene
1072-85-1

o-fluorobromobenzene

2-bromo-1-oxypentafluorosulfanylbenzene
1000995-64-1

2-bromo-1-oxypentafluorosulfanylbenzene

4-bromo-1-oxypentafluorosulfanylbenzene
344455-90-9

4-bromo-1-oxypentafluorosulfanylbenzene

3-bromo-1-oxypentafluorosulfanylbenzene

3-bromo-1-oxypentafluorosulfanylbenzene

C<sub>6</sub>H<sub>3</sub>BrClOSF<sub>5</sub>

C6H3BrClOSF5

C<sub>6</sub>H<sub>3</sub>BrClOSF<sub>5</sub>

C6H3BrClOSF5

C<sub>6</sub>H<sub>3</sub>BrClOSF<sub>5</sub>

C6H3BrClOSF5

C<sub>6</sub>H<sub>3</sub>BrClOSF<sub>5</sub>

C6H3BrClOSF5

C<sub>6</sub>H<sub>3</sub>BrClOSF<sub>5</sub>

C6H3BrClOSF5

C<sub>6</sub>H<sub>3</sub>BrClOSF<sub>5</sub>

C6H3BrClOSF5

C<sub>6</sub>H<sub>3</sub>BrClOSF<sub>5</sub>

C6H3BrClOSF5

C<sub>6</sub>H<sub>3</sub>BrClOSF<sub>5</sub>

C6H3BrClOSF5

C<sub>6</sub>H<sub>3</sub>BrClOSF<sub>5</sub>

C6H3BrClOSF5

C<sub>6</sub>H<sub>3</sub>BrClOSF<sub>5</sub>

C6H3BrClOSF5

C<sub>6</sub>H<sub>4</sub>(OSF<sub>5</sub>)2

C6H4(OSF5)2

C<sub>6</sub>H<sub>4</sub>(OSF<sub>5</sub>)2

C6H4(OSF5)2

C<sub>6</sub>H<sub>4</sub>(OSF<sub>5</sub>)2

C6H4(OSF5)2

3-fluorobromobenzene
1073-06-9

3-fluorobromobenzene

1,3-dibromobenzene
108-36-1

1,3-dibromobenzene

1.4-dibromobenzene
106-37-6

1.4-dibromobenzene

1-Bromo-4-fluorobenzene
460-00-4

1-Bromo-4-fluorobenzene

2,3-dibromobenzene
583-53-9

2,3-dibromobenzene

Conditions
Conditions Yield
With bis(pentafluorosulfur) peroxide; In dichloromethane; at 150 ℃; for 22h;
bromobenzene
108-86-1,52753-63-6

bromobenzene

o-fluorobromobenzene
1072-85-1

o-fluorobromobenzene

2-bromo-1-oxypentafluorosulfanylbenzene
1000995-64-1

2-bromo-1-oxypentafluorosulfanylbenzene

4-bromo-1-oxypentafluorosulfanylbenzene
344455-90-9

4-bromo-1-oxypentafluorosulfanylbenzene

3-bromo-1-oxypentafluorosulfanylbenzene

3-bromo-1-oxypentafluorosulfanylbenzene

C<sub>6</sub>H<sub>3</sub>FBrOSF<sub>5</sub>

C6H3FBrOSF5

C<sub>6</sub>H<sub>3</sub>FBrOSF<sub>5</sub>

C6H3FBrOSF5

C<sub>6</sub>H<sub>3</sub>FBrOSF<sub>5</sub>

C6H3FBrOSF5

C<sub>6</sub>H<sub>3</sub>FBrOSF<sub>5</sub>

C6H3FBrOSF5

C<sub>6</sub>H<sub>3</sub>FBrOSF<sub>5</sub>

C6H3FBrOSF5

C<sub>6</sub>H<sub>3</sub>FBrOSF<sub>5</sub>

C6H3FBrOSF5

C<sub>6</sub>H<sub>3</sub>FBrOSF<sub>5</sub>

C6H3FBrOSF5

C<sub>6</sub>H<sub>3</sub>FBrOSF<sub>5</sub>

C6H3FBrOSF5

C<sub>6</sub>H<sub>3</sub>FBrOSF<sub>5</sub>

C6H3FBrOSF5

C<sub>6</sub>H<sub>3</sub>FBrOSF<sub>5</sub>

C6H3FBrOSF5

C<sub>6</sub>H<sub>4</sub>(OSF<sub>5</sub>)2

C6H4(OSF5)2

C<sub>6</sub>H<sub>4</sub>(OSF<sub>5</sub>)2

C6H4(OSF5)2

C<sub>6</sub>H<sub>4</sub>(OSF<sub>5</sub>)2

C6H4(OSF5)2

3-fluorobromobenzene
1073-06-9

3-fluorobromobenzene

1,3-dibromobenzene
108-36-1

1,3-dibromobenzene

1.4-dibromobenzene
106-37-6

1.4-dibromobenzene

1-Bromo-4-fluorobenzene
460-00-4

1-Bromo-4-fluorobenzene

2,3-dibromobenzene
583-53-9

2,3-dibromobenzene

Conditions
Conditions Yield
With bis(pentafluorosulfur) peroxide; at 100 ℃; for 17h;

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