1218790-63-6 | 2-Propoxy-5-(trifluoromethyl)pyridine-3-boronic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$153.00	$107.00
5g	97%	in stock	$401.00	$281.00
25g	97%	in stock	$914.00	$640.00

Description

• Catalog Number: AA54573
• Chemical Name: 2-Propoxy-5-(trifluoromethyl)pyridine-3-boronic acid
• CAS Number: 1218790-63-6
• Molecular Formula: C9H11BF3NO3
• Molecular Weight: 248.9947
• MDL Number: MFCD15143467
• SMILES: CCCOc1ncc(cc1B(O)O)C(F)(F)F

Computed Properties

• Complexity: 240
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 7
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4

Upstream Synthesis Route

(2-Propoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in the field of organic chemistry due to its unique structure and reactivity.One of the key applications of (2-Propoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid is its utility as a boronic acid derivative in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool in organic synthesis for forming carbon-carbon bonds under mild conditions. By utilizing (2-Propoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid as a coupling partner, chemists can efficiently construct complex organic molecules with high selectivity and yield.Additionally, (2-Propoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid can also serve as a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and materials. Its boronic acid functionality enables the compound to participate in various chemical transformations, allowing for the introduction of the trifluoromethylpyridine moiety into target molecules with precision.Overall, the unique properties of (2-Propoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid make it a valuable tool for chemists engaged in the synthesis of diverse organic compounds with applications across different industries.