252362-02-0 | 4-Chloro-1H-indol-5-amine

Packsize	Purity	Availability	Price	Discounted Price
25mg	95%	in stock	$173.00	$121.00
100mg	95%	in stock	$175.00	$122.00

Description

• Catalog Number: AB51798
• Chemical Name: 4-Chloro-1H-indol-5-amine
• CAS Number: 252362-02-0
• Molecular Formula: C8H7ClN2
• Molecular Weight: 166.6076
• MDL Number: MFCD20682131
• SMILES: Nc1ccc2c(c1Cl)cc[nH]2

Computed Properties

• Complexity: 151
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 2
• XLogP3: 2

Upstream Synthesis Route

4-Chloro-1H-indol-5-amine, also known by its chemical formula C8H7ClN2, is a valuable building block in chemical synthesis with diverse applications in the field of organic chemistry. This compound serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials.In organic synthesis, 4-Chloro-1H-indol-5-amine plays a crucial role as a precursor for the synthesis of indole derivatives, which are important motifs in many biologically active compounds. By undergoing various transformations, such as substitution, addition, and condensation reactions, this compound can be modified to incorporate different functional groups and stereochemistry, enabling the creation of structurally complex molecules with specific properties.Additionally, 4-Chloro-1H-indol-5-amine is widely used in the preparation of heterocyclic compounds, which are prevalent in medicinal chemistry due to their diverse biological activities. This compound can participate in cyclization reactions to form fused ring systems, providing access to a wide range of heterocycles with potential pharmaceutical applications.Furthermore, the presence of the chloro group in 4-Chloro-1H-indol-5-amine offers versatility in further functionalization through selective conversions, allowing for the introduction of additional substituents or reactive sites for subsequent reactions. This flexibility makes it a valuable building block for designing and synthesizing novel chemical entities with tailored properties and functionalities.Overall, the strategic incorporation of 4-Chloro-1H-indol-5-amine into synthetic pathways enables chemists to access a diverse array of compounds with therapeutic, agricultural, and materials science applications, showcasing its significance in the realm of chemical synthesis.