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

CAS No.：850881-09-3

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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
EINECS:
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

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
Fp	110 °C
storage temp.	Keep in dark place,Inert atmosphere,Room temperature
form	clear liquid
color	Colorless to Light yellow

Safety Information

WGK Germany	3
HS Code	2934999090

MSDS Information

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-dioxaborolane Preparation Products And Raw materials

Preparation Products

4,7-Bis(5-broMo-4-hexylthiophen-2-yl)benzo[c][1,2,5]thiadiazole

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