1072951-50-8 | 2-Hydroxy-4-trifluoromethylphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$5.00	$4.00
250mg	98%	in stock	$10.00	$7.00
1g	98%	in stock	$13.00	$10.00
5g	98%	in stock	$49.00	$35.00
10g	98%	in stock	$89.00	$63.00
25g	98%	in stock	$166.00	$117.00
100g	98%	in stock	$466.00	$327.00

Description

• Catalog Number: AD79601
• Chemical Name: 2-Hydroxy-4-trifluoromethylphenylboronic acid
• CAS Number: 1072951-50-8
• Molecular Formula: C7H6BF3O3
• Molecular Weight: 205.9269
• MDL Number: MFCD03094996
• SMILES: OB(c1ccc(cc1O)C(F)(F)F)O

Computed Properties

• Complexity: 197
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 6
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 1

Upstream Synthesis Route

(2-Hydroxy-4-(trifluoromethyl)phenyl)boronic acid is a versatile compound widely used in chemical synthesis for various applications. In organic chemistry, this compound serves as a crucial building block for the preparation of biologically active molecules, pharmaceuticals, agrochemicals, and materials science.As a boronic acid derivative, (2-Hydroxy-4-(trifluoromethyl)phenyl)boronic acid participates in Suzuki-Miyaura cross-coupling reactions, a powerful tool in organic synthesis for forming carbon-carbon bonds. This reaction allows for the efficient construction of complex molecular structures with high selectivity and versatility.Additionally, this compound can be employed in the synthesis of fluorinated organic compounds, which are of interest in medicinal chemistry and materials science due to their unique properties. The trifluoromethyl group in (2-Hydroxy-4-(trifluoromethyl)phenyl)boronic acid enhances the lipophilicity and metabolic stability of the resulting molecules, making them valuable in drug discovery and development.Moreover, (2-Hydroxy-4-(trifluoromethyl)phenyl)boronic acid can be utilized in the preparation of functionalized materials, such as polymers, dendrimers, and organic electronics. Its boronic acid moiety enables it to interact with specific substrates or surfaces, facilitating the modification of materials for various applications in catalysis, sensors, and optoelectronic devices.Overall, the diverse applications of (2-Hydroxy-4-(trifluoromethyl)phenyl)boronic acid in chemical synthesis highlight its importance as a key reagent in the creation of valuable compounds with broad utility in the fields of chemistry and beyond.