CAS 7547-97-9 trans-1-Propen-1-ylboronic acid

NAVIGATION

trans-1-Propen-1-ylboronic acid

PRICE INQUIRY

Catalog Number

ACM7547979-1

CAS Number

7547-97-9

Product Name

trans-1-Propen-1-ylboronic acid

Category

Salt

IUPAC Name

[(E)-prop-1-enyl]boronic acid

Molecular Weight

85.9g/mol

Molecular Formula

C3H7BO2

Canonical SMILES

B(C=CC)(O)O

InChI

InChI=1S/C3H7BO2/c1-2-3-4(5)6/h2-3,5-6H,1H3/b3-2+

InChI Key

CBMCZKMIOZYAHS-NSCUHMNNSA-N

Purity

98%

Application

Trans-1-Propen-1-ylboronic acid serves as a versatile reactant utilized in a range of chemical synthesis applications. It is crucial in palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions and plays a significant role in Cu(II)-mediated Ullmann-type coupling processes. Additionally, it is employed in the preparation of alkynylphenoxyacetic acids, which act as DP2 receptor antagonists for treating allergic inflammatory diseases. This compound is also used in crafting tetrahydrobenzothiophenes, which are conformationally restricted enol-mimic inhibitors of type II dehydroquinase, achieved through Paal-Knorr synthesis involving Suzuki coupling. Furthermore, it facilitates the formation of highly substituted benzannulated cyclooctanol derivatives via samarium diiodide-mediated cyclization and enables the creation of stereospecific dienes through nickel-catalyzed three-component reductive coupling with alkynes and enones.

Complexity

50.8

Covalently-Bonded Unit Count

Exact Mass

86.05391g/mol

Formal Charge

Heavy Atom Count

Monoisotopic Mass

86.05391g/mol

Rotatable Bond Count

If you have any other questions or need other size, please get a quote.