
Catalog Number	AR00EDO4
Chemical Name	6-Chloro-2-methylindole
CAS Number	6127-17-9
Molecular Formula	C9H8ClN
Molecular Weight	165.6195
MDL Number	MFCD09027716
SMILES	Clc1ccc2c(c1)[nH]c(c2)C
NSC Number	115144

6-Chloro-2-methyl-1H-indole serves as a versatile building block in chemical synthesis due to its unique structural properties and reactivity. As a substituted indole compound, it is commonly utilized as a key intermediate in the pharmaceutical industry for the synthesis of various biologically active molecules.In organic chemistry, 6-Chloro-2-methyl-1H-indole can undergo a range of functional group transformations, such as nucleophilic substitution, electrophilic aromatic substitution, and cross-coupling reactions. Its chlorine and methyl substituents provide different sites for further derivatization, allowing for the introduction of diverse functional groups and modifications to tailor the molecule for specific applications.This compound is particularly important in medicinal chemistry and drug development, where indole derivatives are known for their pharmacological properties, including antimicrobial, anticancer, and anti-inflammatory activities. By incorporating 6-Chloro-2-methyl-1H-indole into synthetic pathways, chemists can access novel drug candidates with potential therapeutic benefits.Furthermore, the synthetic accessibility and versatility of 6-Chloro-2-methyl-1H-indole make it a valuable tool for the creation of complex molecular scaffolds in organic synthesis. Its presence in the building blocks library provides researchers with a strategic advantage in designing and constructing target molecules efficiently and with high synthetic yields.