• 1. Evolutionary de novo design of phenothiazine derivatives for dye-sensitized solar cells?
  Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
• 2. Evolution study of photo-synthesized gold nanoparticles by spectral deconvolution model: a quantitative approach
  Chung-Sung Yang,Mong-Shian Shih,Fang-Yi Chang New J. Chem., 2006,30, 729-735
• 3. Excitation energies from ground-state density-functionals by means of generator coordinates
  A. B. F. da Silva,K. Capelle Phys. Chem. Chem. Phys., 2009,11, 4564-4569
• 4. Emerging enantiomeric resolution materials with homochiral nano-fabrications
  Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
• 5. Elusive 2-aminofuran Diels–Alder substrates for a straightforward synthesis of polysubstituted anilines?
  Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyrrolopyridines Pyrrolopyridines
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyrrolopyridines

Comprehensive Overview of 3-Bromo-5-cyano-4-methyl-7-azaindole (CAS No. 1190312-91-4)

3-Bromo-5-cyano-4-methyl-7-azaindole (CAS No. 1190312-91-4) is a specialized heterocyclic compound that has garnered significant attention in pharmaceutical and agrochemical research. This 7-azaindole derivative is characterized by its unique molecular structure, featuring a bromo substituent at the 3-position, a cyano group at the 5-position, and a methyl group at the 4-position. Such structural attributes make it a valuable intermediate in the synthesis of bioactive molecules, particularly in the development of kinase inhibitors and other therapeutic agents.

The growing interest in 3-Bromo-5-cyano-4-methyl-7-azaindole is driven by its potential applications in drug discovery. Researchers are increasingly exploring its utility in targeting protein kinases, which play a critical role in cell signaling pathways. Kinase dysregulation is associated with various diseases, including cancer, inflammation, and neurodegenerative disorders. As a result, compounds like 3-Bromo-5-cyano-4-methyl-7-azaindole are being investigated for their ability to modulate these pathways, offering promising avenues for novel therapeutics.

In addition to its pharmaceutical relevance, 3-Bromo-5-cyano-4-methyl-7-azaindole is also studied for its agrochemical potential. The 7-azaindole scaffold is known for its herbicidal and pesticidal properties, making it a candidate for developing next-generation crop protection agents. With the global push toward sustainable agriculture, the demand for innovative and environmentally friendly agrochemicals is rising, further highlighting the importance of this compound.

From a synthetic chemistry perspective, 3-Bromo-5-cyano-4-methyl-7-azaindole serves as a versatile building block. Its reactive sites, including the bromo and cyano groups, allow for further functionalization through cross-coupling reactions, nucleophilic substitutions, and other transformations. This flexibility enables chemists to tailor the compound for specific applications, enhancing its utility in diverse research fields.

The compound's stability and solubility properties are also noteworthy. 3-Bromo-5-cyano-4-methyl-7-azaindole exhibits moderate solubility in common organic solvents, facilitating its use in laboratory settings. Its stability under standard conditions ensures reliable performance in synthetic workflows, making it a preferred choice for researchers.

As the scientific community continues to explore the potential of 7-azaindole derivatives, 3-Bromo-5-cyano-4-methyl-7-azaindole stands out as a compound with broad applicability. Its role in advancing drug discovery and agrochemical innovation underscores its significance in modern research. For those seeking high-quality intermediates with proven efficacy, this compound represents a compelling option.

In summary, 3-Bromo-5-cyano-4-methyl-7-azaindole (CAS No. 1190312-91-4) is a multifaceted compound with immense potential in both pharmaceutical and agrochemical industries. Its unique structural features, combined with its reactivity and stability, make it a valuable asset for researchers aiming to develop next-generation solutions for global challenges in health and agriculture.

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