1003298-84-7 | 3-Chloro-4-hydroxy-5-methoxyphenylboronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
1g	96%	in stock	$372.00	$260.00
5g	96%	in stock	$1,296.00	$907.00

Description

• Catalog Number: AA01896
• Chemical Name: 3-Chloro-4-hydroxy-5-methoxyphenylboronic acid, pinacol ester
• CAS Number: 1003298-84-7
• Molecular Formula: C13H18BClO4
• Molecular Weight: 284.5436
• MDL Number: MFCD05663844
• SMILES: COc1cc(cc(c1O)Cl)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 321
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2

Upstream Synthesis Route

2-Chloro-6-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (also commonly known as $name$) is a versatile compound utilized in various chemical synthesis processes. This compound plays a crucial role in organic chemistry as a key reagent due to its unique properties and capabilities.In chemical synthesis, $name$ is often employed as a valuable building block for the creation of complex organic molecules. Its functional groups and specific structural features make it an essential component in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. By serving as a precursor or intermediate, $name$ facilitates the formation of intricate molecular structures with high efficiency and precision.Furthermore, the presence of the boron-containing moiety in $name$ enhances its reactivity and compatibility with a wide range of coupling reactions, such as Suzuki-Miyaura cross-coupling. This reactivity profile expands the synthetic possibilities of $name$ and enables chemists to access diverse chemical motifs and scaffolds.Overall, 2-Chloro-6-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol stands as a crucial component in the toolkit of synthetic chemists, offering opportunities for innovative and efficient pathways in the synthesis of valuable chemical compounds.