41492-05-1

  • Product Name1-Bromo-4-butylbenzene
  • MFC10H13Br
  • Molecular Weight213.117
  • Purity99%
  • Appearanceclear colorless to yellow liquid
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Product Details

Quick Details

  • CasNo: 41492-05-1
  • MF: C10H13Br
  • Appearance: clear colorless to yellow liquid
  • Purity: 99%

Buy Quality Sale 1-Bromo-4-butylbenzene 41492-05-1 Efficient Shipping

  • Molecular Formula:C10H13Br
  • Molecular Weight:213.117
  • Appearance/Colour:clear colorless to yellow liquid 
  • Vapor Pressure:0.0503mmHg at 25°C 
  • Refractive Index:n20/D 1.53(lit.)  
  • Boiling Point:243.3 °C at 760 mmHg 
  • Flash Point:109.8 °C 
  • PSA:0.00000 
  • Density:1.242 g/cm3 
  • LogP:3.79170 

1-Bromo-4-butylbenzene(Cas 41492-05-1) Usage

Chemical Properties

clear colorless to yellow liquid

Uses

1-Bromo-4-butylbenzene was used in the preparation of:4-(4-butylphenyl)-2-methylbut-3-yn-2-olteraaza- and hexaazacyclophane4-butyltriphenylamine, monomer required for the preparation of poly(4-butyltriphenylamine)

General Description

Phosphite or phosphine oxide ligand catalyzed Suzuki-Miyaura reaction of 2-pyridyl boron derivatives with 1-bromo-4-butylbenzene has been reported.

Flammability and Explosibility

Notclassified

Consumer Uses

ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

InChI:InChI=1/C10H13Br/c1-2-3-4-9-5-7-10(11)8-6-9/h5-8H,2-4H2,1H3

41492-05-1 Relevant articles

Synthesis method of p-bromo-linear alkylbenzene

-

Paragraph 0035; 0049, (2017/08/25)

The invention belongs to the technical f...

Iron-catalysed, general and operationally simple formal hydrogenation using Fe(OTf)3 and NaBH4

MacNair, Alistair J.,Tran, Ming-Ming,Nelson, Jennifer E.,Sloan, G. Usherwood,Ironmonger, Alan,Thomas, Stephen P.

supporting information, p. 5082 - 5088 (2014/07/08)

An operationally simple and environmenta...

Two flavors of PEPPSI-IPr: Activation and diffusion control in a single NHC-ligated Pd catalyst?

Larrosa, Igor,Somoza, Clara,Banquy, Alexandre,Goldup, Stephen M.

supporting information; experimental part, p. 146 - 149 (2011/03/20)

Abnormal reactivity has been observed in...

Palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides

Shen, Xiaoqiang,Hyde, Alan M.,Buchwald, Stephen L.

scheme or table, p. 14076 - 14078 (2011/01/10)

The palladium-catalyzed conversion of ar...

41492-05-1 Process route

4-n-butylphenyl trifluoromethanesulfonate
1215100-19-8

4-n-butylphenyl trifluoromethanesulfonate

1-butylbenzene
104-51-8

1-butylbenzene

p-bromobutylbenzene
41492-05-1

p-bromobutylbenzene

Conditions
Conditions Yield
With tris-(dibenzylideneacetone)dipalladium(0); triisopropylaluminum diethyl etherate; t-BuBrettPhos; potassium bromide; In toluene; at 100 ℃; Inert atmosphere;
25 %Spectr.
1,4-bromoiodobenzene
589-87-7

1,4-bromoiodobenzene

tri-n-butylindium
15676-66-1

tri-n-butylindium

p-bromobutylbenzene
41492-05-1

p-bromobutylbenzene

Conditions
Conditions Yield
With bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; for 4h; Heating;
80%
tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; Heating;

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