CAS 223919-54-8

1,3,2-Dioxaborolane,2-[(1E)-2-(4-chlorophenyl)ethenyl]-4,4,5,5-tetramethyl-

Description:

1,3,2-Dioxaborolane, 2-[(1E)-2-(4-chlorophenyl)ethenyl]-4,4,5,5-tetramethyl- is a boron-containing organic compound characterized by its dioxaborolane ring structure, which features a five-membered cyclic arrangement containing two oxygen atoms and a boron atom. This compound exhibits unique reactivity due to the presence of the boron atom, which can participate in various chemical reactions, including nucleophilic substitutions and coordination with other molecules. The presence of the 4-chlorophenyl group and the ethenyl substituent contributes to its potential applications in organic synthesis and materials science, particularly in the development of boron-based catalysts or ligands. Additionally, the tetramethyl substituents enhance the compound's stability and solubility in organic solvents. Its specific properties, such as melting point, boiling point, and solubility, would depend on the molecular interactions and the overall structure, making it a subject of interest for further research in synthetic chemistry and potential applications in pharmaceuticals or agrochemicals.

Formula: C₁₄H₁₈BClO₂

2-[2-(4-Chlorophenyl)vinyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 223919-54-8

Formula: C₁₄H₁₈BClO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 264.5555

Ref: IN-DA003C09

(E)-2-(4-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 223919-54-8

(E)-2-(4-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Purity: 99%

Molecular weight: 264.56g/mol

Ref: 54-OR91797

4-Chloro-trans-β-styrylboronic acid pinacol ester

CAS: 223919-54-8

Formula: C₁₄H₁₈BClO₂

Purity: 98%

Molecular weight: 264.56

Ref: 10-F230883