1024017-53-5 | 4-tert-Butoxymethylphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$32.00	$22.00
1g	98%	in stock	$38.00	$27.00
5g	98%	in stock	$100.00	$70.00
25g	98%	in stock	$387.00	$271.00

Description

• Catalog Number: AA09337
• Chemical Name: 4-tert-Butoxymethylphenylboronic acid
• CAS Number: 1024017-53-5
• Molecular Formula: C11H17BO3
• Molecular Weight: 208.0619
• MDL Number: MFCD03701685
• SMILES: OB(c1ccc(cc1)COC(C)(C)C)O

Computed Properties

• Complexity: 181
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4

Upstream Synthesis Route

The versatile compound B-[4-[(1,1-Dimethylethoxy)methyl]phenyl]boronic acid plays a crucial role in chemical synthesis as a valuable building block. Known for its exceptional reactivity and specificity, this boronic acid derivative is utilized in the formation of complex organic molecules through Suzuki-Miyaura cross-coupling reactions.In the realm of organic synthesis, this compound serves as a key component in the construction of biaryl compounds, a class of molecules vital in the pharmaceutical, materials science, and agrochemical industries. By acting as a coupling partner with various aryl halides or pseudohalides in the presence of a palladium catalyst, B-[4-[(1,1-Dimethylethoxy)methyl]phenyl]boronic acid enables the formation of carbon-carbon bonds, leading to the creation of diverse biaryl motifs.Furthermore, this boronic acid derivative exhibits excellent stability and enhanced reactivity under mild reaction conditions, making it an ideal choice for chemists seeking efficient and scalable routes towards synthesizing intricate organic molecules. Its compatibility with a wide range of functional groups further expands its utility in the synthesis of pharmaceutical intermediates and fine chemicals, highlighting its significance in modern chemical research and development efforts.