1005206-25-6 | 4-trifluoromethylthiophenylboronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$15.00	$11.00
250mg	97%	in stock	$35.00	$25.00
5g	97%	in stock	$690.00	$483.00
25g	97%	in stock	$2,982.00	$2,087.00

Description

• Catalog Number: AA02711
• Chemical Name: 4-trifluoromethylthiophenylboronic acid pinacol ester
• CAS Number: 1005206-25-6
• Molecular Formula: C13H16BF3O2S
• Molecular Weight: 304.1361
• MDL Number: MFCD11042448
• SMILES: FC(Sc1ccc(cc1)B1OC(C(O1)(C)C)(C)C)(F)F

Computed Properties

• Complexity: 336
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 20
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2

Upstream Synthesis Route

4,4,5,5-Tetramethyl-2-(4-((trifluoromethyl)thio)phenyl)-1,3,2-dioxaborolane serves as a valuable reagent in chemical synthesis as a boronic acid derivative. This compound is commonly utilized in organic chemistry for its unique reactivity in Suzuki-Miyaura cross-coupling reactions. By acting as a boron source, 4,4,5,5-Tetramethyl-2-(4-((trifluoromethyl)thio)phenyl)-1,3,2-dioxaborolane participates in the formation of carbon-carbon bonds, enabling the efficient construction of complex molecular structures. Its trifluoromethylthiophenyl group imparts specific electronic and steric properties, enhancing its utility for the synthesis of pharmaceuticals, agrochemicals, and advanced materials. This versatile reagent facilitates the generation of diverse chemical entities through its involvement in key synthetic transformations, making it a valuable tool for the preparation of novel compounds for various applications.