CAS 145434-22-6: 2,4,6-TRIISOPROPYLPHENYLBORONIC ACID MET

Description: 2,4,6-Triisopropylphenylboronic acid, with the CAS number 145434-22-6, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a triisopropyl-substituted phenyl ring. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and tetrahydrofuran, while being less soluble in water due to the hydrophobic nature of the isopropyl groups. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis and materials science. Its sterically hindered structure, due to the bulky isopropyl groups, can influence its reactivity and selectivity in chemical transformations. Additionally, this compound may exhibit unique properties related to its electronic structure, which can be leveraged in the development of sensors or catalysts. Proper handling and storage are essential, as with many organoboron compounds, to maintain stability and prevent degradation.

Formula: C₁₇H₂₉BO₂

InChI: InChI=1/C17H29BO2/c1-11(2)14-9-15(12(3)4)17(18(19-7)20-8)16(10-14)13(5)6/h9-13H,1-8H3

Synonyms:

• 2,4,6-Triisopropylphenylboronic acid methyl ester
• Dimethyl [2,4,6-Tris(1-Methylethyl)Phenyl]Boronate

Boronic acid, B-[2,4,6-tris(1-methylethyl)phenyl]-, dimethyl ester

CAS: 145434-22-6

• Formula: C₁₇H₂₉BO₂
• Purity: %
• Color and Shape: Liquid
• Molecular weight: 276.222

2,4,6-Triisopropylphenylboronic acid methyl ester

CAS: 145434-22-6

• Formula: C₁₇H₂₉BO₂
• Purity: 96%
• Color and Shape: colourless liquid
• Molecular weight: 276.22g/mol

2,4,6-Triisopropylphenylboronic acid methyl ester

CAS: 145434-22-6

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• Formula: C₁₇H₂₉BO₂
• Purity: Min. 95%
• Molecular weight: 276.2 g/mol