191171-55-8 | 2-Aminophenylboronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$7.00	$5.00
1g	95%	in stock	$14.00	$10.00
5g	98%	in stock	$31.00	$22.00
10g	95%	in stock	$35.00	$25.00
25g	95%	in stock	$86.00	$61.00
100g	95%	in stock	$266.00	$187.00

Description

• Catalog Number: AB12667
• Chemical Name: 2-Aminophenylboronic acid, pinacol ester
• CAS Number: 191171-55-8
• Molecular Formula: C12H18BNO2
• Molecular Weight: 219.0878
• MDL Number: MFCD02179448
• SMILES: Nc1ccccc1B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 252
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1

Upstream Synthesis Route

The compound 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure makes it highly valuable in various synthetic reactions, particularly in the formation of carbon-carbon and carbon-nitrogen bonds. One of the key applications of $name$ in chemical synthesis is its utilization as a boronic acid derivative for Suzuki-Miyaura cross-coupling reactions. In this reaction, $name$ can serve as a coupling partner with aryl halides or triflates to form biaryl compounds efficiently. This process is widely employed in the pharmaceutical industry, agrochemical synthesis, and material science for the construction of complex molecular structures.Furthermore, $name$ can also be utilized as a fluorescent probe in bioconjugation reactions due to its stable boron-nitrogen bond. This property makes it a valuable tool for labeling biomolecules and studying biological processes.In summary, the compound 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, or $name$, is a versatile reagent in chemical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions and bioconjugation applications.