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1,6-Dibromohexane

  • Product Name: 1,6-Dibromohexane
  • CasNo: 629-03-8
  • Purity:
  • Appearance: Colorless or pale yellow liquid.

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CasNo: 629-03-8

Molecular Formula: C6H12Br2

Appearance: Colorless or pale yellow liquid.

Factory Export Top Purity 1,6-Dibromohexane 629-03-8 In Stock

  • Molecular Formula:C6H12Br2
  • Molecular Weight:243.969
  • Appearance/Colour:Colorless or pale yellow liquid. 
  • Vapor Pressure:0.0483mmHg at 25°C 
  • Melting Point:-2-2.5 °C(lit.) 
  • Refractive Index:n20/D 1.507(lit.)  
  • Boiling Point:244.1 °C at 760 mmHg 
  • Flash Point:110.8 °C 
  • PSA:0.00000 
  • Density:1.584 g/cm3 
  • LogP:3.33660 

1,6-Dibromohexane(Cas 629-03-8) Usage

Preparation

1,6-Dibromohexane is synthesized from hexanediol by bromination.

InChI:InChI=1/C6H12Br2/c7-5-3-1-2-4-6-8/h1-6H2

629-03-8 Relevant articles

Stable and easily available sulfide surrogates allow a stereoselective activation of alcohols

Brutiu, Bogdan R.,Drescher, Martina,Matya?ovsky, Ján,Maulide, Nuno,Merad, Jérémy,Pinto, Alexandre,Stopka, Tobias

, p. 7770 - 7774 (2021/06/16)

Isothiouronium salts are easily accessib...

Triphenylphosphine-N-bromosuccinimide mediated chemoselective cyclodehydration of diols

Zhao, Shuo,Wu, You,Sun, Qi,Cheng, Tie-Ming,Li, Run-Tao

, p. 1154 - 1162 (2015/04/14)

A triphenylphosphine-N-bromosuccinimide ...

Biomolecule interaction using atomic force microscope

-

Page/Page column, (2014/03/26)

The present patent application describes...

Primary alkyl bromides from dimethylthiocarbamates

Moynihan, Meghan F.,Tucker, Joseph W.,Abelt, Christopher J.

experimental part, p. 3565 - 3568 (2009/06/18)

The conversion of primary alkyl dimethyl...

629-03-8 Process route

O-6-(tetrahydro-2H-pyran-2-yloxy)hexyl dimethylcarbamothioate
1110667-75-8

O-6-(tetrahydro-2H-pyran-2-yloxy)hexyl dimethylcarbamothioate

1 ,6-dibromohexane
629-03-8

1 ,6-dibromohexane

2-[(6-bromohexyl)oxy]tetrahydro-2H-pyran
53963-10-3

2-[(6-bromohexyl)oxy]tetrahydro-2H-pyran

1-bromo-6-hexanol
4286-55-9

1-bromo-6-hexanol

C<sub>7</sub>H<sub>13</sub>BrO<sub>2</sub>
1110667-79-2

C7H13BrO2

Conditions
Conditions Yield
With 4-(bromomethylene)morpholin-4-ium bromide; In dichloromethane; at 0 ℃; for 1.5h; Inert atmosphere;
27%
23%
14%
5%
1,6-hexanediol
629-11-8

1,6-hexanediol

1 ,6-dibromohexane
629-03-8

1 ,6-dibromohexane

1-bromo-6-hexanol
4286-55-9

1-bromo-6-hexanol

Conditions
Conditions Yield
With hydrogen bromide; In toluene; for 13h; Heating;
79%
With hydrogen bromide; In toluene; for 24h; Heating;
69%
1%

629-03-8 Upstream products

  • 629-11-8
    629-11-8

    1,6-hexanediol

  • 592-42-7
    592-42-7

    1,5-Hexadien

  • 109-64-8
    109-64-8

    1,3-dibromo-propane

  • 10035-10-6
    10035-10-6

    hydrogen bromide

629-03-8 Downstream products

  • 52559-88-3
    52559-88-3

    1,5,12,16-tetrathia-cyclodocosane

  • 56496-17-4
    56496-17-4

    7-azoniaspiro<6.6>tridecane bromide

  • 50592-87-5
    50592-87-5

    1-bromo-6-methoxyhexane

  • 13179-98-1
    13179-98-1

    1,6-dimethoxyhexane

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