CAS 1138450-30-2: [1-Methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]boronic acid

Description: [1-Methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and other nucleophiles. This compound features a pyrazole ring, which contributes to its aromatic stability and potential reactivity. The trifluoromethyl group enhances its lipophilicity and can influence its electronic properties, making it useful in various chemical reactions, including Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. The methyl group on the pyrazole ring can also affect the compound's solubility and reactivity. As a boronic acid, it is typically used in medicinal chemistry and materials science, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure and functional groups make it a valuable intermediate in synthetic pathways, allowing for the introduction of diverse functionalities into target molecules.

Formula: C₅H₆BF₃N₂O₂

InChI: InChI=1S/C5H6BF3N2O2/c1-11-2-3(6(12)13)4(10-11)5(7,8)9/h2,12-13H,1H3

Synonyms:

• 1-Methyl-3-(trifluoromethyl)pyrazole-4-boronic acid

Boronic acid, B-[1-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]-

CAS: 1138450-30-2

• Formula: C₅H₆BF₃N₂O₂
• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 193.9195

(1-Methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl)boronic acid

CAS: 1138450-30-2

• Purity: 95.0%
• Molecular weight: 193.9199981689453

1-Methyl-3-(trifluoromethyl)pyrazole-4-boronic acid

CAS: 1138450-30-2

• Purity: 98%
• Molecular weight: 193.92

1-Methyl-3-trifluoromethylpyrazole-4-boronic acid

CAS: 1138450-30-2

• Purity: 0.99
• Molecular weight: 193.92g/mol

[1-Methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]boronic acid

CAS: 1138450-30-2

Versatile small molecule scaffold

• Formula: C₅H₆BF₃N₂O₂
• Purity: Min. 95%
• Molecular weight: 193.92 g/mol