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