1693-86-3

  • Product Name:3-Hexylthiophene
  • Molecular Formula:C10H16S
  • Purity:99%
  • Molecular Weight:168.303
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Product Details;

CasNo: 1693-86-3

Molecular Formula: C10H16S

Appearance: colorless transparent or light yellow liquid

factory and supplier 1693-86-3 3-Hexylthiophene in stock

  • Molecular Formula:C10H16S
  • Molecular Weight:168.303
  • Appearance/Colour:colorless transparent or light yellow liquid 
  • Vapor Pressure:0.128mmHg at 25°C 
  • Melting Point:-39.15°C (estimate) 
  • Refractive Index:n20/D 1.496(lit.)  
  • Boiling Point:225.6 °C at 760 mmHg 
  • Flash Point:64.2 °C 
  • PSA:28.24000 
  • Density:0.946 g/cm3 
  • LogP:3.87090 

3-Hexylthiophene(Cas 1693-86-3) Usage

Preparation

The 2,5-dibromo-3-dodecylthiophene was dissolved in tetrahydromyran, added with methylmagnesium bromide, preheated and added with catalyst for reaction reaction was injected into alcohol solvent, and hexane was added to remove the copolymer, and then the mixture was soxhlet filtered using chloroform, and the chloroform layer was evaporated and concentrated to obtain a purple membrane; the purple membrane was vacuum filtered to obtain the product 3-hexylthiophene.

General Description

3-Hexylthiophene, a sulfur containing heterocyclic building block, is a thiophene derivative. Poly(3-hexylthiophene) (P3HT) nanofibres have been used for the preparation of organic phototransistors (OPTs).

InChI:InChI=1/C10H16S/c1-2-3-4-5-6-10-7-8-11-9-10/h7-9H,2-6H2,1H3

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1693-86-3 Process route

3-Bromothiophene
872-31-1

3-Bromothiophene

1-bromo-hexane
111-25-1

1-bromo-hexane

3,3'-bithiophene
3172-56-3

3,3'-bithiophene

3-(1-methylpentyl)thiophene
740804-46-0

3-(1-methylpentyl)thiophene

3-hexylthiophene
1693-86-3

3-hexylthiophene

Conditions
Conditions Yield
1-bromo-hexane; n-hexylmagnesium bromide; With magnesium; In 2-methyltetrahydrofuran; at 60 - 85 ℃; for 4.5h;
3-Bromothiophene; 1,3-bis[(diphenylphosphino)propane]dichloronickel(II); In 2-methyltetrahydrofuran; at 15 - 20 ℃; for 20h;
With hydrogenchloride; water; In 2-methyltetrahydrofuran; Product distribution / selectivity;
97.5 - 98.88 %Chromat.
0.37 - 0.45 %Chromat.
0.15 - 0.49 %Chromat.
3-Bromothiophene
872-31-1

3-Bromothiophene

n-hexylmagnesium bromide
3761-92-0

n-hexylmagnesium bromide

3,3'-bithiophene
3172-56-3

3,3'-bithiophene

3-hexylthiophene
1693-86-3

3-hexylthiophene

Conditions
Conditions Yield
bis(triphenylphosphine)nickel(II) chloride; In tetrahydrofuran; at 0 - 60 ℃; for 2.5h; Product distribution / selectivity;
36.2 - 82.7 %Chromat.
6.4 - 27.1 %Chromat.
bis-triphenylphosphine-palladium(II) chloride; In diethyl ether; at 20 ℃; for 2.5h; Product distribution / selectivity;
4.0 - 4.5 %Chromat.
0.2 - 0.5 %Chromat.
bis(triphenylphosphine)nickel(II) chloride; In diethyl ether; at 20 ℃; for 1h; Product distribution / selectivity;
1.7 - 3.1 %Chromat.
0.5 - 6.3 %Chromat.
In diethyl ether; at 20 ℃; for 1h; Conversion of starting material;
0.5 - 1.1 %Chromat.
0.2 - 0.4 %Chromat.

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