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3-Hexylthiophene-2-boronic acid pinacol ester_Molecular_structure_CAS_850881-09-3)
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3-Hexylthiophene-2-boronic acid pinacol ester

Catalog No. 697400 Name Sigma Aldrich
CAS Number 850881-09-3 Website http://www.sigmaaldrich.com
M. F. C16H27BO2S Telephone 1-800-521-8956
M. W. 294.26038 Fax
Purity 95% Email
Storage Chembase ID: 141524

SYNONYMS

Title
3-己基噻吩-2-硼酸频哪醇酯
IUPAC name
2-(3-hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
IUPAC Traditional name
2-(3-hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Synonyms
3-Hexyl-2-thienylboronic acid
2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
2-(3-己基-2-噻吩基)-4,4,5,5-四甲基-1,3,2-二氧杂硼烷

DATABASE IDS

CAS Number 850881-09-3
MDL Number MFCD11045447

PROPERTIES

Empirical Formula (Hill Notation) C16H27BO2S
Purity 95%
Density 0.983 g/mL at 25 °C
Flash Point >110 °C
Flash Point >230 °F
Refractive Index n20/D 1.490-1.499
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, half-mask respirator (US), multi-purpose combination respirator cartridge (US)
German water hazard class 3

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application
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 for dye-sensitized solar cells7
Description (简体中文)
包装
1, 5 g in glass bottle
Application
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 for dye-sensitized solar cells7

REFERENCES