1072811-21-2 | 4-Methoxyindole-2-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$69.00	$49.00
1g	95%	in stock	$182.00	$128.00
5g	95%	in stock	$606.00	$425.00

Description

• Catalog Number: AD40418
• Chemical Name: 4-Methoxyindole-2-boronic acid pinacol ester
• CAS Number: 1072811-21-2
• Molecular Formula: C15H20BNO3
• Molecular Weight: 273.1352
• MDL Number: MFCD11858387
• SMILES: COc1cccc2c1cc([nH]2)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 358
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 20
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2

Upstream Synthesis Route

4-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole, commonly known as $name$, is a versatile compound widely used in chemical synthesis. This compound is utilized as a valuable building block for the construction of complex molecules due to its unique structure and reactivity. In organic synthesis, $name$ serves as a key intermediate for the functionalization of indole derivatives through various chemical transformations such as Suzuki-Miyaura cross-coupling reactions. By incorporating $name$ into a synthetic pathway, chemists can efficiently access a diverse array of indole-based compounds with tailored properties and functionalities. Additionally, the presence of the boronate ester moiety in $name$ enables selective and mild derivatization strategies, making it a valuable tool for the synthesis of pharmaceuticals, agrochemicals, and materials with specific molecular architectures. The application of 4-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole in chemical synthesis offers synthetic chemists a powerful and versatile tool for achieving complex molecular targets with precision and efficiency.