• 1. Examination of ammonia–poly(pyrrole) interactions by piezoelectric and conductivity measurements
  Analyst, 1991,116, 1125-1130
• 2. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
  Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
• 3. Excellent energy storage performance in NaNbO3-based relaxor antiferroeic ceramics under a low electric field
  XuxinCheng,XiaomingChen,PengyuanFan
• 4. Emerging 2D hybrid nanomaterials: towards enhanced sensitive and selective conductometric gas sensors at room temperature
  Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
• 5. Embedding cyclic nitrone in mesoporous silica particles for EPR spin trapping of superoxide and other radicals?
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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Aminopyridines and derivatives

Comprehensive Overview of 6-Bromo-2-methylpyridin-3-amine (CAS No. 126325-47-1): Properties, Applications, and Industry Insights

6-Bromo-2-methylpyridin-3-amine (CAS No. 126325-47-1) is a specialized heterocyclic compound with a pyridine backbone, widely recognized for its role in pharmaceutical intermediates and agrochemical synthesis. This compound features a bromine substituent at the 6-position and a methyl group at the 2-position, which contribute to its unique reactivity and versatility in organic transformations. Researchers and industries value it for its potential in designing bioactive molecules, particularly in drug discovery and material science.

The growing demand for 6-Bromo-2-methylpyridin-3-amine is driven by its applications in catalysis and cross-coupling reactions, such as Suzuki-Miyaura or Buchwald-Hartwig couplings. These reactions are pivotal in creating complex organic frameworks for API development (Active Pharmaceutical Ingredients). Recent trends highlight its utility in small-molecule inhibitors targeting kinases, a hot topic in cancer research and precision medicine. Users searching for "pyridine derivatives in drug design" or "brominated amine synthesis" will find this compound highly relevant.

From a synthetic chemistry perspective, CAS No. 126325-47-1 offers excellent regioselectivity, making it a preferred building block for high-value intermediates. Its stability under mild conditions aligns with the industry's shift toward green chemistry and sustainable synthesis. Environmental concerns and regulatory pressures have increased searches for "eco-friendly bromination methods" and "low-toxicity pyridine analogs," positioning this compound as a candidate for innovation.

In material science, 6-Bromo-2-methylpyridin-3-amine contributes to the development of organic semiconductors and ligand systems for metal-organic frameworks (MOFs). These applications resonate with trending topics like "next-gen electronic materials" and "MOFs for carbon capture." Its structural adaptability allows integration into photovoltaic materials, addressing the surge in interest around renewable energy technologies.

Quality control and analytical standards for CAS No. 126325-47-1 are critical, given its use in high-purity applications. Advanced techniques like HPLC and NMR spectroscopy ensure batch consistency, a frequent concern for buyers searching for "certified pyridine derivatives." Suppliers emphasizing GMP compliance and traceability gain traction in B2B markets.

Future prospects for 6-Bromo-2-methylpyridin-3-amine include expanding its role in bioconjugation and proteomics, areas gaining momentum due to advancements in antibody-drug conjugates (ADCs). As AI-driven drug discovery accelerates, queries like "AI-optimized heterocycles" underscore the need for structurally diverse libraries, where this compound excels.

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