The Chemical Backbone: Understanding 3-(4-Chlorbutyl)-1H-indol-5-carbonitril in Synthesis
In the intricate world of chemical synthesis, specific molecules serve as the fundamental building blocks for creating complex, high-value compounds. 3-(4-Chlorbutyl)-1H-indol-5-carbonitril, identified by CAS number 143612-79-7, is one such pivotal intermediate, particularly significant in the pharmaceutical industry. Understanding its chemical structure, properties, and synthetic applications is crucial for researchers and manufacturers aiming for precision and efficiency in their processes.
The molecule's structure is characterized by an indole ring system, a core component in many natural products and pharmaceuticals, substituted with a nitrile group at the 5-position and a 4-chlorobutyl chain at the 3-position. This particular arrangement provides reactive sites that are highly amenable to various chemical transformations. The nitrile group can be hydrolyzed to a carboxylic acid or reduced to an amine, while the terminal chlorine atom on the butyl chain is a good leaving group, facilitating nucleophilic substitution reactions. These functionalities make 3-(4-Chlorbutyl)-1H-indol-5-carbonitril an exceptionally versatile starting material for organic chemists.
Its prominent role as a Vilazodone intermediate highlights its importance. Vilazodone, an antidepressant, requires a carefully constructed molecular backbone, and this indole derivative provides precisely the necessary structural elements. The ability to source this compound with high purity, often above 97%, from reliable manufacturers is essential for achieving the desired yield and purity of the final API. When searching for this chemical, terms like 'buy 3-(4-Chlorbutyl)-1H-indol-5-carbonitril,' 'CAS 143612-79-7 manufacturer,' or 'high purity indole intermediate' are commonly used by industry professionals.
Beyond its pharmaceutical applications, 3-(4-Chlorbutyl)-1H-indol-5-carbonitril is a valuable tool in broader organic synthesis research. Its indole scaffold can be further elaborated through electrophilic aromatic substitution, C-H functionalization, or cross-coupling reactions, opening pathways to novel compounds with potential applications in materials science or agrochemicals. Researchers often look for suppliers who can offer not only standard products but also support for custom synthesis projects involving complex indole derivatives.
As a leading supplier, we emphasize the quality and reliability of our chemical intermediates. The consistent availability of 3-(4-Chlorbutyl)-1H-indol-5-carbonitril, sourced from our advanced manufacturing facilities, ensures that our clients can proceed with their synthetic endeavors with confidence. Understanding the chemical nuances of such intermediates allows us to better serve the needs of the research and industrial communities, facilitating innovation and progress.
In conclusion, 3-(4-Chlorbutyl)-1H-indol-5-carbonitril (CAS 143612-79-7) stands as a testament to the critical role of well-defined chemical intermediates in driving scientific advancement. Its versatile reactivity and importance in pharmaceutical synthesis make it a key molecule for any advanced chemical research or manufacturing operation.
Perspectives & Insights
Agile Reader One
“The nitrile group can be hydrolyzed to a carboxylic acid or reduced to an amine, while the terminal chlorine atom on the butyl chain is a good leaving group, facilitating nucleophilic substitution reactions.”
Logic Vision Labs
“These functionalities make 3-(4-Chlorbutyl)-1H-indol-5-carbonitril an exceptionally versatile starting material for organic chemists.”
Molecule Origin 88
“Vilazodone, an antidepressant, requires a carefully constructed molecular backbone, and this indole derivative provides precisely the necessary structural elements.”