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647020

Sigma-Aldrich

2,2′-Bithiophene-5,5′-diboronic acid bis(pinacol) ester

97%

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About This Item

Empirical Formula (Hill Notation):
C20H28B2O4S2
CAS Number:
Molecular Weight:
418.19
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

208-212 °C (lit.)

SMILES string

CC1(C)OB(OC1(C)C)c2ccc(s2)-c3ccc(s3)B4OC(C)(C)C(C)(C)O4

InChI

1S/C20H28B2O4S2/c1-17(2)18(3,4)24-21(23-17)15-11-9-13(27-15)14-10-12-16(28-14)22-25-19(5,6)20(7,8)26-22/h9-12H,1-8H3

InChI key

XWWXVHGWYCXJCJ-UHFFFAOYSA-N

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Taichi Ikeda et al.
Nanoscale, 8(30), 14673-14681 (2016-07-21)
Oligomers of tetra(ethylene glycol)-disubstituted phenyl-capped bithiophene (Ph2TPh) linked by catechol and resorcinol were prepared. Catechol and resorcinol link the monomers via the ortho- and meta-positions of the benzene ring, respectively, and function as turning points in the folding process of

Articles

Oligothiophenes are important organic electronic materials which can be produced using synthetic intermediates and Suzuki coupling.

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