1073353-99-7 | 5-Chloro-2-nitrophenylboronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
1g	96%	in stock	$251.00	$176.00
5g	96%	in stock	$946.00	$662.00

Description

• Catalog Number: AD45384
• Chemical Name: 5-Chloro-2-nitrophenylboronic acid, pinacol ester
• CAS Number: 1073353-99-7
• Molecular Formula: C12H15BClNO4
• Molecular Weight: 283.5158
• MDL Number: MFCD11053894
• SMILES: CC1(C)OB(OC1(C)C)c1cc(Cl)ccc1[N+](=O)[O-]

Computed Properties

• Complexity: 355
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1

Upstream Synthesis Route

The compound 2-(5-Chloro-2-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile reagent commonly employed in chemical synthesis. Its unique structure allows for selective reactions, making it a valuable tool in organic chemistry.This boron-containing compound can participate in various cross-coupling reactions, facilitating the formation of carbon-carbon bonds. It is often utilized in Suzuki-Miyaura coupling reactions, where it serves as a boron source to couple with different aryl or vinyl halides. These reactions enable the construction of complex organic molecules efficiently and with high selectivity.Furthermore, 2-(5-Chloro-2-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is known for its stability and compatibility with a wide range of reaction conditions. Its presence can enhance the reactivity of certain substrates, leading to improved yields and purity in the final products.Overall, this compound is a valuable synthetic building block in the toolkit of chemical researchers, enabling the efficient and controlled synthesis of diverse organic molecules with potential applications in pharmaceuticals, materials science, and agrochemicals.