1132669-91-0 | 4-Chloro-2-formylphenylboronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$48.00	$33.00
1g	98%	in stock	$58.00	$40.00
5g	98%	in stock	$173.00	$121.00
25g	98%	in stock	$572.00	$400.00
100g	98%	in stock	$1,535.00	$1,074.00

Description

• Catalog Number: AE25202
• Chemical Name: 4-Chloro-2-formylphenylboronic acid, pinacol ester
• CAS Number: 1132669-91-0
• Molecular Formula: C13H16BClO3
• Molecular Weight: 266.5283399999999
• MDL Number: MFCD18731001
• SMILES: O=Cc1cc(Cl)ccc1B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 316
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2

Upstream Synthesis Route

5-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is a versatile compound commonly utilized in chemical synthesis. Its unique structure allows for selective functionalization and the creation of complex molecules with precise control.In organic synthesis, 5-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde serves as a key building block for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its boron-containing moiety enables Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in a controlled and efficient manner.Furthermore, this compound plays a crucial role in the synthesis of biologically active compounds and innovative materials. Its chloro-substituted benzaldehyde group provides a handle for further modifications, allowing chemists to tailor the structure of the final product for specific applications.Overall, the use of 5-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde in chemical synthesis enables researchers to explore new avenues in drug development, materials science, and other fields requiring the precise construction of organic molecules.