1217501-14-8 | 3-Butoxy-4-methoxyphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$137.00	$96.00
5g	98%	in stock	$386.00	$270.00
10g	98%	in stock	$665.00	$466.00
25g	98%	in stock	$1,317.00	$922.00

Description

• Catalog Number: AA53968
• Chemical Name: 3-Butoxy-4-methoxyphenylboronic acid
• CAS Number: 1217501-14-8
• Molecular Formula: C11H17BO4
• Molecular Weight: 224.0613
• MDL Number: MFCD13195649
• SMILES: CCCCOc1cc(ccc1OC)B(O)O

Computed Properties

• Complexity: 189
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 6

Upstream Synthesis Route

(3-Butoxy-4-methoxyphenyl)boronic acid, also known as $name$, is a versatile and valuable compound used in chemical synthesis. With its boronic acid functional group, this molecule serves as a key building block in a variety of organic reactions, particularly in the field of Suzuki-Miyaura cross-coupling reactions.In chemical synthesis, (3-Butoxy-4-methoxyphenyl)boronic acid acts as a highly effective reagent for forming carbon-carbon bonds. When combined with suitable partners like aryl halides or triflates and a palladium catalyst, this compound undergoes a cross-coupling reaction to create biaryl compounds. These biaryl compounds are prevalent in pharmaceuticals, agrochemicals, and materials science, making (3-Butoxy-4-methoxyphenyl)boronic acid a critical intermediate in the production of these important products.Additionally, the unique properties of boronic acids allow for the functionalization of organic molecules, enabling chemists to introduce new substituents and enhance the diversity of molecules synthesized. This versatility makes (3-Butoxy-4-methoxyphenyl)boronic acid a valuable tool for the creation of complex organic compounds in chemical research and industrial applications.Overall, (3-Butoxy-4-methoxyphenyl)boronic acid plays a crucial role in modern chemical synthesis, offering a reliable and efficient method for constructing carbon-carbon bonds and facilitating the development of innovative molecules with various applications.