Basic information Safety Supplier Related

2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Basic information Safety Supplier Related

2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Basic information

Product Name:
2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Synonyms:
  • 2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 3-Hexyl-2-thiopheneboronic Acid Pinacol Ester
  • 3-Hexyl-2-thiopheneboronic acid pinacol ester
  • 2-(3-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 3-Hexylthiophene-2-boronic acid pinacol ester 95%
  • 3-hydroxy-2,3-dimethylbutan-2-yl hydrogen (3-hexylthiophen-2-yl)boronate
  • 2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 3-Hexylthiophene-2-boronic acid pinacol ester
  • 3-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene
CAS:
850881-09-3
MF:
C16H27BO2S
MW:
294.26
Product Categories:
  • Boronate Esters
  • Boronic Acids and Derivatives
  • Chemical Synthesis
  • Heteroaryl Boronate Esters
  • Materials Science
  • Organic and Printed Electronics
  • Organometallic Reagents
  • Synthetic Tools and Reagents
  • Thiophene Monomers and Building Blocks
Mol File:
850881-09-3.mol
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2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Chemical Properties

Boiling point:
385.3±30.0 °C(Predicted)
Density 
0.983 g/mL at 25 °C
refractive index 
n20/D 1.492
Flash point:
110 °C
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
clear liquid
color 
Colorless to Light yellow
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Safety Information

WGK Germany 
3
HS Code 
2934999090
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2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Usage And Synthesis

Uses

Reagent used for• ;Suzuki-Miyaura cross-coupling reactions1 • ;p-type/n-type switching of ambipolar bithiazole-benzothiadiazole-based polymers in solar cells1 • ;Hierarchical self-assembly of semiconductor functionalized peptide a-helixes and optoelectronic properties2 Reagent used in Preparation of• ;Photovoltaic materials, polymers, and thiophene-based compounds with photophysical, electrochemical, and fluorescent properties3,4,5• ;Polymer solar cells for Low band gap poly(1,4-arylene-2,5-thienylene)s with benzothiadiazole units6 • ;Dithienothiophene-based dyes

Uses

Reagent used for

  • Suzuki-Miyaura cross-coupling reactions
  • p-type/n-type switching of ambipolar bithiazole-benzothiadiazole-based polymers in solar cells
  • Hierarchical self-assembly of semiconductor functionalized peptide a-helixes and optoelectronic properties

Reagent used in Preparation of
  • Photovoltaic materials, polymers, and thiophene-based compounds with photophysical, electrochemical, and fluorescent properties
  • Polymer solar cells for Low band gap poly(1,4-arylene-2,5-thienylene)s with benzothiadiazole units
  • Dithienothiophene-based dyes for dye-sensitized solar cells

2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneSupplier

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