1010836-19-7 | 2-Carboxythiophene-4-boronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	96%	in stock	$105.00	$74.00
1g	96%	in stock	$249.00	$175.00
5g	96%	in stock	$712.00	$498.00
10g	96%	in stock	$1,178.00	$824.00
25g	96%	in stock	$2,111.00	$1,478.00

Description

• Catalog Number: AA04593
• Chemical Name: 2-Carboxythiophene-4-boronic acid, pinacol ester
• CAS Number: 1010836-19-7
• Molecular Formula: C11H15BO4S
• Molecular Weight: 254.1104
• MDL Number: MFCD08064045
• SMILES: OC(=O)c1scc(c1)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 315
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2

Upstream Synthesis Route

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid, commonly used in chemical synthesis, serves as a versatile building block in the creation of novel organic compounds. With its unique structure and reactivity, this compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials science. Specifically, it acts as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in a controlled and efficient manner. This important transformation allows chemists to access a wide range of structurally diverse molecules, facilitating the discovery of new drugs, functional materials, and biologically active compounds. Additionally, the presence of boron in this molecule provides opportunities for further functionalization and modification, expanding its utility in the realm of organic synthesis.