1072812-35-1 | 3-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-indole

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$299.00	$209.00
1g	98%	in stock	$713.00	$499.00

Description

• Catalog Number: AD76161
• Chemical Name: 3-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-indole
• CAS Number: 1072812-35-1
• Molecular Formula: C15H20BNO2
• Molecular Weight: 257.1358
• MDL Number: MFCD16995768
• SMILES: Cc1c([nH]c2c1cccc2)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 342
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1

Upstream Synthesis Route

3-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole, also known as $name$, is a versatile compound that is widely used in chemical synthesis for various applications. In chemical synthesis, $name$ serves as a valuable building block for the construction of complex organic molecules. It is commonly employed as a key reagent in the synthesis of pharmaceuticals, agrochemicals, and materials with specific properties. One of the main applications of $name$ in chemical synthesis is in cross-coupling reactions, particularly in Suzuki-Miyaura coupling. This reaction enables the formation of carbon-carbon bonds under mild conditions, making it a powerful tool for the synthesis of biaryl compounds, which are prevalent in drug discovery and material science.$name$ is also utilized in the production of functionalized indole derivatives, which are important scaffolds in medicinal chemistry due to their diverse biological activities. By incorporating $name$ into synthetic routes, chemists can access a wide range of indole-containing molecules with tailored properties for various applications.Moreover, $name$ can participate in transition-metal catalyzed reactions, such as palladium-catalyzed cross-coupling reactions, enabling the selective formation of C-C bonds at specific positions in the molecule. This allows for the rapid assembly of complex molecular structures with high efficiency and selectivity.Overall, the application of 3-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole in chemical synthesis offers synthetic chemists a versatile and efficient strategy for the construction of intricate organic molecules with diverse functionalities and applications.