86626-38-2 | 4-Bromoindoline

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$15.00	$11.00
5g	97%	in stock	$68.00	$48.00
10g	97%	in stock	$128.00	$90.00
25g	97%	in stock	$311.00	$218.00

Description

• Catalog Number: AB66985
• Chemical Name: 4-Bromoindoline
• CAS Number: 86626-38-2
• Molecular Formula: C8H8BrN
• Molecular Weight: 198.0598
• MDL Number: MFCD07371633
• SMILES: Brc1cccc2c1CCN2

Computed Properties

• Complexity: 126
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• XLogP3: 2.6

Upstream Synthesis Route

4-Bromoindoline is a versatile organic compound that finds wide application in chemical synthesis, particularly in the field of medicinal chemistry. This compound serves as a key building block in the development of various pharmaceuticals and agrochemicals due to its unique structural properties and reactivity. Incorporating 4-Bromoindoline into a molecule can often enhance its biological activity or introduce specific functionalities that are crucial for target binding.In organic synthesis, 4-Bromoindoline can act as a valuable starting material for the construction of complex molecules through various synthetic strategies such as cross-coupling reactions, electrophilic substitutions, and cycloadditions. Its bromine substituent enables selective transformations at that position, allowing chemists to control the regioselectivity and stereochemistry of the final product. Additionally, the presence of the indoline moiety provides a versatile functional group that can undergo further modifications to tailor the molecule's properties.Furthermore, 4-Bromoindoline derivatives have shown promising potential in the development of new drugs for treating various diseases, including cancer, neurological disorders, and infectious diseases. By judiciously designing and synthesizing molecules based on 4-Bromoindoline, researchers can explore novel chemical space and optimize the pharmacokinetic and pharmacodynamic profiles of drug candidates. Its compatibility with modern synthetic methods and bioconjugation strategies makes it a valuable asset in drug discovery and development efforts.