76347-13-2 | 2-Isopropylboronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$7.00	$5.00
5g	95%	in stock	$19.00	$14.00
10g	95%	in stock	$23.00	$17.00
25g	95%	in stock	$42.00	$30.00

Description

• Catalog Number: AB62433
• Chemical Name: 2-Isopropylboronic acid, pinacol ester
• CAS Number: 76347-13-2
• Molecular Formula: C9H19BO2
• Molecular Weight: 170.0570
• MDL Number: MFCD05663856
• SMILES: CC(B1OC(C(O1)(C)C)(C)C)C

Computed Properties

• Complexity: 159
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

2-Isopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a valuable compound used in chemical synthesis as a boron source. It serves as a versatile building block in organic chemistry, particularly in the field of metal-catalyzed cross-coupling reactions. This compound is commonly utilized as a boron reagent in the Suzuki-Miyaura coupling reaction, a powerful tool for forming carbon-carbon bonds.In organic synthesis, 2-Isopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane can be employed to introduce boron functionality into various organic molecules. It enables the selective and efficient formation of new carbon-carbon bonds, facilitating the synthesis of complex organic compounds such as pharmaceuticals, agrochemicals, and materials.Additionally, this compound can participate in diverse transformations, including palladium-catalyzed C-C bond formations, which are crucial in the creation of natural products and advanced materials. Its unique structure and reactivity make it a valuable reagent for chemists seeking to construct intricate molecular architectures with precision and efficiency.