882562-40-5 | 3-(2,5-Dichloropyrimidin-4-yl)-1-(phenylsulfonyl)-1h-indole

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$37.00	$26.00

Description

• Catalog Number: AC02568
• Chemical Name: 3-(2,5-Dichloropyrimidin-4-yl)-1-(phenylsulfonyl)-1h-indole
• CAS Number: 882562-40-5
• Molecular Formula: C18H11Cl2N3O2S
• Molecular Weight: 404.2698
• MDL Number: MFCD17392847
• SMILES: Clc1ncc(c(n1)c1cn(c2c1cccc2)S(=O)(=O)c1ccccc1)Cl

Computed Properties

• Complexity: 594
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 26
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• XLogP3: 4.8

Upstream Synthesis Route

3-(2,5-Dichloropyrimidin-4-yl)-1-(phenylsulfonyl)-1H-indole is a versatile compound that finds considerable utility in chemical synthesis, particularly in the field of medicinal chemistry. Its unique structure and reactivity make it a valuable building block for the construction of complex molecules with potential biological activity. One of the key applications of this compound is in the development of novel pharmaceuticals. By serving as a key intermediate in the synthesis of biologically active molecules, 3-(2,5-Dichloropyrimidin-4-yl)-1-(phenylsulfonyl)-1H-indole plays a crucial role in pharmaceutical research and drug discovery. It enables chemists to access diverse structural motifs and optimize the properties of potential drug candidates.Furthermore, this compound can be utilized in the preparation of fluorescent dyes and labeled probes for biological imaging studies. Its ability to undergo selective transformations allows for the attachment of various functional groups that can impart specific properties for use in imaging applications. This makes 3-(2,5-Dichloropyrimidin-4-yl)-1-(phenylsulfonyl)-1H-indole a valuable tool in the development of molecular probes for studying biological systems.In addition, the presence of both a pyrimidine and an indole moiety in this compound offers opportunities for the design and synthesis of new heterocyclic scaffolds with potential biological activity. By incorporating 3-(2,5-Dichloropyrimidin-4-yl)-1-(phenylsulfonyl)-1H-indole into molecular frameworks, chemists can explore structure-activity relationships and optimize the properties of bioactive compounds for various applications in medicinal chemistry.Overall, the versatility and synthetic accessibility of 3-(2,5-Dichloropyrimidin-4-yl)-1-(phenylsulfonyl)-1H-indole make it a valuable building block for chemical synthesis, particularly in the development of pharmaceuticals, fluorescent probes, and biologically active molecules. Its role in enabling the construction of complex molecular architectures underscores its importance in advancing research and innovation in the field of chemistry and medicinal sciences.