1072951-37-1 | 2,4,6-Trifluoro-3-hydroxyphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$50.00	$35.00
250mg	98%	in stock	$63.00	$44.00
1g	98%	in stock	$129.00	$90.00
5g	98%	in stock	$605.00	$423.00
25g	98%	in stock	$2,376.00	$1,664.00

Description

• Catalog Number: AB54770
• Chemical Name: 2,4,6-Trifluoro-3-hydroxyphenylboronic acid
• CAS Number: 1072951-37-1
• Molecular Formula: C6H4BF3O3
• Molecular Weight: 191.9004
• MDL Number: MFCD11053885
• SMILES: OB(c1c(F)cc(c(c1F)O)F)O

Computed Properties

• Complexity: 183
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 6
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 1

Upstream Synthesis Route

The (2,4,6-Trifluoro-3-hydroxyphenyl)boronic acid is a valuable chemical reagent commonly utilized in organic synthesis processes. As an aromatic boronic acid derivative, this compound plays a crucial role in the formation of carbon-carbon and carbon-heteroatom bonds in various chemical reactions. Its trifluoromethyl and hydroxyl substituents confer unique properties and reactivity, making it a versatile tool in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.(2,4,6-Trifluoro-3-hydroxyphenyl)boronic acid is particularly prized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, where it serves as a key component in the construction of biaryl compounds. By engaging in these catalyzed coupling reactions, this boronic acid helps chemists to efficiently link aromatic rings together, enabling the creation of structurally complex molecules with precise control over regioselectivity and stereoselectivity.Moreover, the hydroxyl group present in the (2,4,6-Trifluoro-3-hydroxyphenyl)boronic acid molecule offers additional functionality, facilitating further derivatization or transformation via simple chemical manipulations. This allows for the introduction of additional functional groups or modifications, enabling the fine-tuning of properties in target molecules.Overall, the use of (2,4,6-Trifluoro-3-hydroxyphenyl)boronic acid in chemical synthesis provides chemists with a powerful tool for constructing intricate molecular architectures with high efficiency and precision, making it an indispensable component in modern organic chemistry research and development.