1186398-35-5 | 5-Formyl-2-methylphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$48.00	$33.00
250mg	95%	in stock	$57.00	$40.00
1g	95%	in stock	$145.00	$102.00
5g	95%	in stock	$502.00	$352.00
10g	95%	in stock	$813.00	$569.00
25g	95%	in stock	$1,591.00	$1,114.00

Description

• Catalog Number: AD74340
• Chemical Name: 5-Formyl-2-methylphenylboronic acid
• CAS Number: 1186398-35-5
• Molecular Formula: C8H9BO3
• Molecular Weight: 163.9663
• MDL Number: MFCD16295249
• SMILES: O=Cc1ccc(c(c1)B(O)O)C

Computed Properties

• Complexity: 160
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2

Upstream Synthesis Route

The (5-Formyl-2-methylphenyl)boronic acid is a versatile reagent commonly used in chemical synthesis for a variety of applications. Its specific structural features make it a valuable building block in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. In cross-coupling reactions, this compound acts as a key component in the Suzuki-Miyaura coupling reaction, a widely used method for forming aryl-aryl bonds. The boronic acid functionality facilitates the coupling of the aryl group with various electrophiles, leading to the synthesis of biaryl compounds with high efficiency and selectivity.Furthermore, the aldehyde group present in the molecule allows for diverse functionalization through various chemical transformations. It can be readily converted into different functional groups such as alcohols, acids, and amines, providing access to a wide range of structurally complex molecules.Overall, the (5-Formyl-2-methylphenyl)boronic acid plays a crucial role in modern synthetic chemistry by enabling the efficient construction of complex molecular structures with high precision and control. Its versatility and reactivity make it an indispensable tool for chemists working in the field of organic synthesis.