CAS 2121512-35-2: 2-(2-Bromo-6-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description: 2-(2-Bromo-6-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique dioxaborolane structure, which features a five-membered ring containing boron and oxygen atoms. This compound typically exhibits a high degree of stability due to the presence of the boron atom, which can participate in various chemical reactions, including Suzuki coupling reactions, making it valuable in organic synthesis and materials science. The presence of the bromo and chloro substituents on the phenyl ring enhances its reactivity and allows for further functionalization. Additionally, the tetramethyl groups contribute to the compound's steric bulk, influencing its solubility and reactivity. This compound is likely to be a solid at room temperature and may have specific applications in pharmaceuticals or agrochemicals due to its structural properties. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks.

Formula: C₁₂H₁₅BBrClO₂

InChI: InChI=1S/C12H15BBrClO2/c1-11(2)12(3,4)17-13(16-11)10-8(14)6-5-7-9(10)15/h5-7H,1-4H3

InChI key: InChIKey=DLQOZPQKJXCYSY-UHFFFAOYSA-N

SMILES: ClC1=CC=CC(Br)=C1B2OC(C)(C)C(O2)(C)C

Synonyms:

• 2-(2-Bromo-6-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• 1,3,2-Dioxaborolane, 2-(2-bromo-6-chlorophenyl)-4,4,5,5-tetramethyl-

1,3,2-Dioxaborolane, 2-(2-bromo-6-chlorophenyl)-4,4,5,5-tetramethyl-

CAS: 2121512-35-2

• Formula: C₁₂H₁₅BBrClO₂
• Purity: 95%
• Molecular weight: 317.4143

2-Bromo-6-chlorophenylboronic acid pinacol ester

CAS: 2121512-35-2

• Purity: 97%
• Molecular weight: 317.4100036621094

2-Bromo-6-chlorophenylboronic acid pinacol ester

CAS: 2121512-35-2

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• Formula: C₁₂H₁₅BBrClO₂
• Purity: Min. 95%
• Molecular weight: 317.41 g/mol