1150271-60-5 | 5-(Ethoxycarbonyl)thiophene-2-boronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$356.00	$249.00
1g	98%	in stock	$783.00	$548.00

Description

• Catalog Number: AA20164
• Chemical Name: 5-(Ethoxycarbonyl)thiophene-2-boronic acid, pinacol ester
• CAS Number: 1150271-60-5
• Molecular Formula: C13H19BO4S
• Molecular Weight: 282.1636
• MDL Number: MFCD11855979
• SMILES: CCOC(=O)c1ccc(s1)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 343
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4

Upstream Synthesis Route

Ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate is a versatile chemical compound commonly used in chemical synthesis procedures. This compound serves as a valuable building block in the creation of various organic molecules due to its unique structure and reactivity.When incorporated into chemical reactions, Ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate acts as a key precursor for the introduction of functional groups such as thiophene and boron-containing moieties. These functional groups play significant roles in drug discovery, material science, and agrochemical development.In organic synthesis, this compound can be utilized in cross-coupling reactions, palladium-catalyzed coupling reactions, and Suzuki-Miyaura coupling reactions to create complex organic structures efficiently. Its presence enables the formation of carbon-carbon bonds, which are essential for the construction of diverse chemical compounds.Overall, Ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate facilitates the preparation of intricate molecules with specific functionalities, making it a valuable tool in the realm of chemical synthesis.