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4-Bromochlorobenzene

  • Product Name: 4-Bromochlorobenzene
  • CasNo: 106-39-8
  • Purity:
  • Appearance: white to almost white crystalline powder

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CasNo： 106-39-8

Molecular Formula： C6H4BrCl

Appearance： white to almost white crystalline powder

Purity 99% Min 4-Bromochlorobenzene 106-39-8 Spot Supply with Safe Transportation

  • Molecular Formula:C6H4BrCl
  • Molecular Weight:191.455
  • Appearance/Colour:white to almost white crystalline powder 
  • Vapor Pressure:0.674mmHg at 25°C 
  • Melting Point:64-67 °C(lit.) 
  • Refractive Index:1,496-1,498 
  • Boiling Point:192.651 °C at 760 mmHg 
  • Flash Point:78.434 °C 
  • PSA：0.00000 
  • Density:1.628 g/cm3; 
  • LogP:3.10250 

4-Bromochlorobenzene(Cas 106-39-8) Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 86, p. 964, 1964 DOI: 10.1021/ja01059a073The Journal of Organic Chemistry, 55, p. 3415, 1990 DOI: 10.1021/jo00297a087

InChI:InChI=1/C6H4BrCl/c7-5-1-3-6(8)4-2-5/h1-4H

106-39-8 Relevant articles

-

Derbyshire,Waters

, p. 573,576 (1950)

-

Mild chlorination of aromatic compounds with tin(IV) chloride and lead tetraacetate

Muathen, Hussni A.

, p. 8863 - 8866 (1996)

SnCl4/Pb(OAc)4 acts as a safe source of ...

Eco-compatible zeolite-catalysed continuous halogenation of aromatics

Losch,Kolb,Astafan,Daou,Pinard,Pale,Louis

, p. 4714 - 4724 (2016)

A completely eco-compatible halogenation...

Bromination of Deactivated Aromatics Using BrF3 without a Catalyst

Rozen, Shlomo,Lerman, Ori

, p. 239 - 240 (1993)

-

Highly para-Selective Mono-Chlorination of Aromatic Compounds Under Mild Conditions by t-Butyl Hypochlorite in the Presence of Zeolites

Smith, Keith,Butters, Michael,Nay, Barry

, p. 1157 - 1158 (1985)

t-Butyl hypochlorite supported on H(1+),...

-

Kovacic,Sparks

, p. 5740 (1960)

-

-

Gokel et al.

, p. 1633 (1977)

-

Decarboxylative Ipso Halogenation of Mercury(II) Pyridinecarboxylates. Facile Formation of 3-Iodo- and 3-Bromopyridines

Uemura, Sakae,Tanaka, Sakuya,Okano, Masaya,Hamana, Masatomo

, p. 3297 - 3301 (1983)

Treatment of mercury(II) nicotinate with...

Poly-N-bromosulfonamide-melamine as a novel brominating reagent for regioselective ipso-bromination of arylboronic acids

Alavinia, Sedigheh,Ghorbani-Vaghei, Ramin

, p. 1269 - 1276 (2021/08/27)

A practical synthetic method for the syn...

The graphite-catalyzed: ipso -functionalization of arylboronic acids in an aqueous medium: metal-free access to phenols, anilines, nitroarenes, and haloarenes

Badgoti, Ranveer Singh,Dandia, Anshu,Parewa, Vijay,Rathore, Kuldeep S.,Saini, Pratibha,Sharma, Ruchi

, p. 18040 - 18049 (2021/05/29)

An efficient, metal-free, and sustainabl...

Orthogonal Stability and Reactivity of Aryl Germanes Enables Rapid and Selective (Multi)Halogenations

Deckers, Kristina,Fricke, Christoph,Schoenebeck, Franziska

supporting information, p. 18717 - 18722 (2020/08/25)

While halogenation is of key importance ...

Metal- and base-free synthesis of aryl bromides from arylhydrazines

Phuc Tran, Dat,Nomoto, Akihiro,Mita, Soichiro,Dong, Chun-ping,Kodama, Shintaro,Mizuno, Takumi,Ogawa, Akiya

supporting information, (2020/05/08)

An efficient method was developed to syn...

106-39-8 Process route

1-chloro-1,2,3,4,5,6-hexabromocyclohexane
88400-64-0

1-chloro-1,2,3,4,5,6-hexabromocyclohexane

toluene
108-88-3,15644-74-3,16713-13-6

toluene

bromochlorobenzene
106-39-8

bromochlorobenzene

1-bromo-3-chlorobenzene
108-37-2

1-bromo-3-chlorobenzene

2-bromo-1-chlorobenzene
694-80-4

2-bromo-1-chlorobenzene

benzyl bromide
100-39-0

benzyl bromide

1,1'-(1,2-ethanediyl)bisbenzene
103-29-7

1,1'-(1,2-ethanediyl)bisbenzene

chlorobenzene
108-90-7

chlorobenzene

Conditions
Conditions Yield
at 55 ℃; for 16h; Product distribution; Irradiation; other solvents;
bromobenzene
108-86-1,52753-63-6

bromobenzene

bromochlorobenzene
106-39-8

bromochlorobenzene

2-bromo-1-chlorobenzene
694-80-4

2-bromo-1-chlorobenzene

2-nitrophenyl bromide
577-19-5

2-nitrophenyl bromide

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

Conditions
Conditions Yield
With Nitryl chloride; trifluoroacetic acid; at 20 ℃; for 8h; Product distribution; Mechanism;

106-39-8 Upstream products

  • 108-86-1
    108-86-1

    bromobenzene

  • 64-17-5
    64-17-5

    ethanol

  • 17333-85-6
    17333-85-6

    4-chlorophenyldiazonium salt

  • 17333-82-3
    17333-82-3

    4-bromo-benzenediazonium ion

106-39-8 Downstream products

  • 74-11-3
    74-11-3

    para-chlorobenzoic acid

  • 7005-72-3
    7005-72-3

    4-chlorodiphenyl ether

  • 3061-36-7
    3061-36-7

    1,4-diphenoxybenzene

  • 106-46-7
    106-46-7

    para-dichlorobenzene

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