1004761-68-5 | 4-Amino-3,5-dimethylphenylboronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$33.00	$23.00
250mg	95%	in stock	$56.00	$39.00
1g	95%	in stock	$103.00	$72.00
5g	95%	in stock	$364.00	$255.00
25g	95%	in stock	$1,763.00	$1,234.00

Description

• Catalog Number: AA02487
• Chemical Name: 4-Amino-3,5-dimethylphenylboronic acid, pinacol ester
• CAS Number: 1004761-68-5
• Molecular Formula: C14H22BNO2
• Molecular Weight: 247.1410
• MDL Number: MFCD18837628
• SMILES: CC1(C)OB(OC1(C)C)c1cc(C)c(c(c1)C)N

Computed Properties

• Complexity: 291
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1

Upstream Synthesis Route

The compound 2,6-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is a versatile and valuable building block in chemical synthesis. It is commonly used as a key reagent in organic reactions, particularly in the field of medicinal and materials chemistry.This compound is known for its unique structure, which allows it to participate in a variety of important transformations. One of its primary applications is as a ligand in transition metal-catalyzed coupling reactions, such as Suzuki-Miyaura cross-coupling. In this process, the aniline moiety serves as an important directing group, enabling the selective formation of new carbon-carbon bonds.Furthermore, the boron-containing group attached to the aniline scaffold can undergo various transformations, making it a valuable handle for further functionalization. This feature enables chemists to introduce a wide range of substituents, allowing for the tailored synthesis of complex molecules.Overall, the compound 2,6-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline plays a crucial role in modern chemical synthesis, facilitating the efficient construction of diverse organic structures with applications in drug discovery, materials science, and beyond.