CAS 942069-65-0

3-Chloro-5-(trifluoromethyl)benzeneboronic acid pinacol ester

Description:

3-Chloro-5-(trifluoromethyl)benzeneboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid moiety esterified with pinacol, alongside a chloro and a trifluoromethyl group on a benzene ring. This compound typically exhibits properties such as moderate solubility in organic solvents and stability under standard laboratory conditions. The trifluoromethyl group contributes to its lipophilicity and can influence its reactivity in cross-coupling reactions, making it valuable in synthetic organic chemistry, particularly in the formation of carbon-carbon bonds. The boronic acid functionality allows for participation in Suzuki-Miyaura coupling reactions, which are widely used for constructing complex organic molecules. Additionally, the presence of the chlorine atom can serve as a leaving group or participate in further functionalization. Overall, this compound is significant in medicinal chemistry and materials science due to its versatile reactivity and potential applications in drug development and organic synthesis.

Synonyms:

• 3-Chloro-5-(trifluoromethyl)phenylboronic acid pinacol ester

3-Chloro-5-(trifluoromethyl)phenylboronic acid, pinacol ester

CAS: 942069-65-0

Formula: C₁₃H₁₅BClF₃O₂

Purity: 97%

Color and Shape: Liquid

Molecular weight: 306.5162

Ref: IN-DA003ETL

2-[3-Chloro-5-(trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 942069-65-0

2-[3-Chloro-5-(trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Purity: 98%

Color and Shape: Clear Oil

Molecular weight: 306.52g/mol

Ref: 54-PC48619

2-(3-Chloro-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 942069-65-0

Formula: C₁₃H₁₅BClF₃O₂

Purity: 97%

Molecular weight: 306.52

Ref: 10-F219700