578878
2,2′−Bithiophene-5-boronic acid pinacol ester
Synonym(s):
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,2′-bithiophene
About This Item
Recommended Products
refractive index
n20/D 1.5900 (lit.)
Quality Level
mp
35.5-38.0 °C (average)
SMILES string
CC1(C)OB(OC1(C)C)c2ccc(s2)-c3cccs3
InChI
1S/C14H17BO2S2/c1-13(2)14(3,4)17-15(16-13)12-8-7-11(19-12)10-6-5-9-18-10/h5-9H,1-4H3
InChI key
HPOQARMSOPOZMW-UHFFFAOYSA-N
Related Categories
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
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Articles
Oligothiophenes are important organic electronic materials which can be produced using synthetic intermediates and Suzuki coupling.
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
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