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850881-09-3

850881-09-3 Structure

850881-09-3 Structure
IdentificationBack Directory
[Name]

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

850881-09-3
[Synonyms]

3-Hexyl-2-thienylboronic acid
3-Hexyl-2-thiopheneboronic acid pinacol ester
3-Hexylthiophene-2-boronic acid pinacol ester
3-Hexylthiophene-2-boronic acid pinacol ester 95%
2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
1,3,2-Dioxaborolane, 2-(3-hexyl-2-thienyl)-4,4,5,5-tetramethyl-
3-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene
2-(3-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
3-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene>
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-Hexyl-2-thiopheneboronic Acid Pinacol Ester
[Molecular Formula]

C16H27BO2S
[MDL Number]

MFCD11045447
[MOL File]

850881-09-3.mol
[Molecular Weight]

294.26
Chemical PropertiesBack Directory
[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
[InChI]

InChI=1S/C16H27BO2S/c1-6-7-8-9-10-13-11-12-20-14(13)17-18-15(2,3)16(4,5)19-17/h11-12H,6-10H2,1-5H3
[InChIKey]

XCXAUPBHQCCWCI-UHFFFAOYSA-N
[SMILES]

O1C(C)(C)C(C)(C)OB1C1SC=CC=1CCCCCC
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H312-H332
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501
[WGK Germany ]

3
[HS Code ]

2934999090
[Storage Class]

10 - Combustible liquids
Hazard InformationBack Directory
[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
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