110543-98-1 | Ethyl 5-acetoxy-6-bromo-2-(bromomethyl)-1-methyl-1h-indole-3-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$24.00	$17.00
25g	97%	in stock	$50.00	$35.00
100g	97%	in stock	$129.00	$90.00
500g	97%	in stock	$449.00	$315.00

Description

• Catalog Number: AB73895
• Chemical Name: Ethyl 5-acetoxy-6-bromo-2-(bromomethyl)-1-methyl-1h-indole-3-carboxylate
• CAS Number: 110543-98-1
• Molecular Formula: C15H15Br2NO4
• Molecular Weight: 433.0919
• MDL Number: MFCD00407019
• SMILES: CCOC(=O)c1c(CBr)n(c2c1cc(OC(=O)C)c(c2)Br)C

Computed Properties

• Complexity: 434
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 22
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• XLogP3: 3.3

Upstream Synthesis Route

The compound Ethyl 5-acetoxy-6-bromo-2-(bromomethyl)-1-methyl-1H-indole-3-carboxylate holds significant importance in chemical synthesis due to its versatile applications in organic chemistry. This compound serves as a valuable building block for the construction of complex molecules through various synthetic routes.Ethyl 5-acetoxy-6-bromo-2-(bromomethyl)-1-methyl-1H-indole-3-carboxylate can be utilized as a key intermediate in the synthesis of pharmaceutical compounds, agrochemicals, and functional materials. Its unique structure enables the introduction of diverse functional groups, facilitating the modification and tailoring of its chemical properties for specific applications.In organic synthesis, this compound can participate in numerous reactions such as nucleophilic substitutions, palladium-catalyzed coupling reactions, and other transformations to access a wide range of derivatives with desired characteristics. Its bromoalkyl and ester functionalities offer strategic points for further elaboration and diversification, enabling the synthesis of novel compounds with enhanced biological or physicochemical properties.