2113-57-7

  • Product Name:3-Bromobiphenyl
  • Molecular Formula:C12H9Br
  • Purity:99%
  • Molecular Weight:233.107
Inquiry

Product Details

pd_meltingpoint:9oC

Appearance:Colorless to pale yellow liquid

Purity:99%

Quality Manufacturer Supply High Purity 99% 3-Bromobiphenyl 2113-57-7 with Reasonable Price

  • Molecular Formula:C12H9Br
  • Molecular Weight:233.107
  • Appearance/Colour:Colorless to pale yellow liquid 
  • Vapor Pressure:0.00205mmHg at 25°C 
  • Melting Point:9oC 
  • Refractive Index:1.637-1.641  
  • Boiling Point:300 °C at 760 mmHg 
  • Flash Point:135.6 °C 
  • PSA:0.00000 
  • Density:1.363 g/cm3 
  • LogP:4.11610 

3-Bromobiphenyl(Cas 2113-57-7) Usage

synthesis

Add 1-bromo-3-iodobenzene (4.67 g, 16.5mmol), phenylboronic acid (1.83 g, 15.0 mmol), Pd (OAc)2 (101 mg, 0.450 mmol), PPh3 (239 mg, 0.911 mmol), and K2CO3 (6.23 g, 45.1 mmol) to a 200 mL twonecked round-bottom flask. Add toluene (40 mL) and water (40 mL) via syringe and reflux the mixture (bath temp. 100°C) for 24 h. Extract the resulting mixture with ethyl acetate (30 mL x 3). Dry the combined organic layer over Na2SO4 and concentrate in vacuo. Purify the residue to silica gel column chromatography (eluent:hexane).

Synthesis Reference(s)

The Journal of Organic Chemistry, 41, p. 24, 1976 DOI: 10.1021/jo00863a005

Air & Water Reactions

Insoluble in water.

Reactivity Profile

3-Bromobiphenyl may be sensitive to light. 3-Bromobiphenyl may react with oxidizing materials.

Fire Hazard

Flash point data for 3-Bromobiphenyl are not available. 3-Bromobiphenyl is probably combustible.

General Description

Clear yellow viscous liquid. Insoluble in water.

InChI:InChI=1/C12H9Br/c13-12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H

2113-57-7 Relevant articles

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Mowry et al.

, p. 1916 (1948)

-

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Lichtin,Leftin

, p. 4207 (1952)

-

Synthesis and catalytic activity of nickel(II) complexes containing NCN pincer ligands

Nair, Ashwin G.,McBurney, Roy T.,Gatus, Mark R.D.,Walker, D.Barney,Bhadbhade, Mohan,Messerle, Barbara A.

, p. 63 - 70 (2017)

In this study, nickel(II) complexes [Lme...

-

de la Mare,Hassan

, p. 3004,3006 (1957)

-

The photochemistry of polyhaloarenes XIII. The photohydrodehalogenation of 3,4-dibromobiphenyl

Freeman, Peter K.,Jang, Jung-Suk,Haugen, Christian M.

, p. 8397 - 8406 (1996)

Irradiation of 3,4-dibromobiphenyl (BpBr...

-

Huber et al.

, p. 1109,1111 (1946)

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Synthesis, Structure, and Chiroptical Properties of Indolo- and Pyridopyrrolo-Carbazole-Based C2-Symmetric Azahelicenes

Taniguchi, Taisei,Nishii, Yuji,Mori, Tadashi,Nakayama, Ken-ichi,Miura, Masahiro

supporting information, p. 7356 - 7361 (2021/04/26)

Treatment of 11,12-bis(1,1’-biphenyl-3-y...

Facile synthesis of NC(sp3)O pincer palladium complexes and their use as efficient catalysts for Suzuki-Miyaura reaction of aryl bromides in aqueous medium

Gong, Jun-Fang,Li, Nan,Pan, Ya-Ping,Song, Mao-Ping,Yang, Jing-Jing,Zhu, Zhi-Wu

, (2020/12/15)

Two NC(sp3)O pincer palladium(II) comple...

METHOD OF PRODUCING HALOGEN COMPOUND

-

Paragraph 0052-0060, (2021/05/07)

PROBLEM TO BE SOLVED: To provide a metho...

Palladium (II)–Salan Complexes as Catalysts for Suzuki–Miyaura C–C Cross-Coupling in Water and Air. Effect of the Various Bridging Units within the Diamine Moieties on the Catalytic Performance

Bunda, Szilvia,Joó, Ferenc,Kathó, ágnes,Udvardy, Antal,Voronova, Krisztina

supporting information, (2020/09/18)

Water-soluble salan ligands were synthes...

2113-57-7 Process route

iodobenzene
591-50-4

iodobenzene

(3-bromophenyl)boronic acid
89598-96-9

(3-bromophenyl)boronic acid

3,3'-dibromobiphenyl
16400-51-4

3,3'-dibromobiphenyl

3-bromobiphenyl
2113-57-7

3-bromobiphenyl

Conditions
Conditions Yield
With potassium phosphate; [N,N,O]-tridentate unsymmetrical Schiff base Au(I); In o-xylene; for 3h;
With potassium phosphate; C44H44N3O2PdPolSi; In 5,5-dimethyl-1,3-cyclohexadiene; water; at 130 ℃; for 3h; solid phase reaction;
bromobenzene
108-86-1,52753-63-6

bromobenzene

N-sulphinylphenylhydrazine
17420-03-0

N-sulphinylphenylhydrazine

2-Bromobiphenyl
2052-07-5

2-Bromobiphenyl

4-bromo-1,1'-biphenyl
92-66-0

4-bromo-1,1'-biphenyl

3-bromobiphenyl
2113-57-7

3-bromobiphenyl

diphenyldisulfane
882-33-7

diphenyldisulfane

Conditions
Conditions Yield
at 135 ℃; for 72h; Further byproducts given;
12.7%
6.9%
20.9%
1.1%
at 135 ℃; for 72h; Further byproducts given;
19.5%
12.9%
1.1%
8.1%

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