108847-76-3 | Thianthrene-1-boronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$15.00	$10.00
1g	97%	in stock	$18.00	$12.00
5g	97%	in stock	$18.00	$13.00
10g	97%	in stock	$33.00	$24.00
25g	97%	in stock	$78.00	$55.00
100g	97%	in stock	$256.00	$180.00

Description

• Catalog Number: AB58770
• Chemical Name: Thianthrene-1-boronic acid
• CAS Number: 108847-76-3
• Molecular Formula: C12H9BO2S2
• Molecular Weight: 260.1397
• MDL Number: MFCD00093039
• SMILES: OB(c1cccc2c1Sc1ccccc1S2)O

Computed Properties

• Complexity: 277
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

Thianthren-1-ylboronic acid is a highly valuable chemical reagent in organic synthesis. It serves as a versatile building block for the creation of various functionalized molecules with applications across different fields of chemistry. This boronic acid derivative is particularly prized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, where it can be coupled with a wide range of aryl halides or pseudohalides. This reaction is widely used in medicinal chemistry, material science, and agrochemical research for the construction of complex organic structures. Additionally, Thianthren-1-ylboronic acid can also be employed in the formation of C-C and C-N bonds through a variety of palladium-catalyzed coupling reactions, enabling the synthesis of pharmaceutical intermediates, fine chemicals, and functionalized materials. Its unique structural and reactivity properties make Thianthren-1-ylboronic acid an indispensable tool for chemists seeking to access diverse chemical space and develop innovative synthetic routes.