1011460-69-7 | (4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanamine

Packsize	Purity	Availability	Price	Discounted Price
50mg	95%	1 week	$634.00	$444.00
100mg	95%	1 week	$907.00	$635.00
250mg	95%	1 week	$1,258.00	$881.00
500mg	95%	1 week	$1,937.00	$1,356.00
1g	95%	1 week	$2,464.00	$1,725.00

Description

• Catalog Number: AA04776
• Chemical Name: (4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanamine
• CAS Number: 1011460-69-7
• Molecular Formula: C14H22BNO2
• Molecular Weight: 247.141
• MDL Number: MFCD18730174
• SMILES: NCc1ccc(c(c1)B1OC(C(O1)(C)C)(C)C)C

Upstream Synthesis Route

The organic compound (4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanamine, also known as $name$, is a versatile building block widely utilized in chemical synthesis. Its unique structure containing a boronate ester group makes it a valuable reagent in various organic transformations.$name$ is commonly employed in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, where it serves as a nucleophilic partner to form carbon-carbon bonds. This reaction is pivotal in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and materials.Additionally, $name$ finds application in the construction of functionalized heterocycles through palladium-catalyzed reactions. Its strategic incorporation enables the introduction of diverse functional groups with high efficiency and selectivity, facilitating the synthesis of diverse chemical entities.Moreover, $name$ can participate in other transformations like C-H activation, aromatic substitution, and metal-catalyzed cross-coupling reactions, showcasing its adaptability in modern organic synthesis strategies. Its robust reactivity and compatibility with a range of substrates make it a valuable tool for chemists working in the field of organic synthesis.