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2-Thienylboronic acid

Catalog Number
ACM6165680-1
CAS Number
6165-68-0
Product Name
2-Thienylboronic acid
Structure
Category
Salt
IUPAC Name
thiophen-2-ylboronic acid
Molecular Weight
127.96g/mol
Molecular Formula
C4H5BO2S
Canonical SMILES
B(C1=CC=CS1)(O)O
InChI
InChI=1S/C4H5BO2S/c6-5(7)4-2-1-3-8-4/h1-3,6-7H
InChI Key
ARYHTUPFQTUBBG-UHFFFAOYSA-N
Application
2-Thienylboronic acid, a white to light yellow crystal powder, is primarily utilized in various chemical reactions and processes. It serves as a critical reagent in Palladium-catalyzed Suzuki-Miyaura cross-couplings and is essential for alkylation, boration, coupling reactions, Suzuki coupling, and halogenation of fluorenyl bromide. Additionally, it plays a significant role in the chain-growth catalyst transfer polycondensation of conjugated alternating copolymers. Furthermore, it is employed in ferric perchlorate-promoted reactions with fullerenes to produce fullerenyl boronic esters.
Complexity
78.4
Covalently-Bonded Unit Count
1
EC Number
612-186-6
Exact Mass
128.010331g/mol
Formal Charge
0
Heavy Atom Count
8
Monoisotopic Mass
128.010331g/mol
Rotatable Bond Count
1
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