• 1. Evolution of shape, size, and areal density of a single plane of Si nanocrystals embedded in SiO2 matrix studied by atom probe tomography
  Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
• 2. Emergence of microfluidic wearable technologies
  Joo Chuan Yeo,Kenry Lab Chip, 2016,16, 4082-4090
• 3. 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
• 4. Embedding heteroatoms: an effective approach to create porphyrin-based functional materials
  Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
• 5. Enabling stable MnO2 matrix for aqueous zinc-ion battery cathodes?
  Yiding Jiao,Liqun Kang,Jasper Berry-Gair,Kit McColl,Jianwei Li,Haobo Dong,Hao Jiang,Ryan Wang,Furio Corà,Dan J. L. Brett,Ivan P. Parkin J. Mater. Chem. A, 2020,8, 22075-22082

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Aminopyridines and derivatives

Comprehensive Guide to 3-(2-Aminopyridin-3-yl)propan-1-ol (CAS No. 89226-78-8): Properties, Applications, and Market Insights

3-(2-Aminopyridin-3-yl)propan-1-ol (CAS No. 89226-78-8) is a specialized organic compound with significant applications in pharmaceuticals, agrochemicals, and material science. This aminopyridine derivative is known for its unique structural features, which make it a valuable intermediate in synthetic chemistry. The compound's molecular formula is C₈H₁₂N₂O, and it features both an amino group and a hydroxyl group, enabling diverse reactivity.

The growing interest in 3-(2-Aminopyridin-3-yl)propan-1-ol is driven by its role in drug discovery, particularly in the development of kinase inhibitors and other bioactive molecules. Researchers frequently search for "aminopyridine derivatives in drug design" or "CAS 89226-78-8 applications," highlighting its relevance in modern medicinal chemistry. Its structural versatility allows for modifications that enhance binding affinity and selectivity in target proteins.

In agrochemical applications, 3-(2-Aminopyridin-3-yl)propan-1-ol serves as a precursor for crop protection agents. With increasing global demand for sustainable agriculture, queries like "eco-friendly agrochemical intermediates" and "CAS 89226-78-8 in crop science" reflect its potential. The compound's ability to act as a chelating agent further broadens its utility in formulations aimed at improving nutrient uptake in plants.

From a synthetic perspective, the compound's hydroxyl and amino functional groups facilitate reactions such as esterification, amidation, and condensation. Laboratories often explore "synthetic routes for 3-(2-Aminopyridin-3-yl)propan-1-ol" or "CAS 89226-78-8 purity standards" to optimize production processes. High-purity grades of this compound are essential for reproducible results in research and industrial applications.

The market for 3-(2-Aminopyridin-3-yl)propan-1-ol is expanding, driven by advancements in pharmaceutical R&D and agrochemical innovations. Trends such as "green chemistry in intermediate synthesis" and "cost-effective aminopyridine derivatives" are shaping procurement strategies. Suppliers are increasingly focusing on scalable and sustainable production methods to meet the demands of global markets.

Analytical techniques like HPLC, NMR, and mass spectrometry are critical for characterizing 3-(2-Aminopyridin-3-yl)propan-1-ol. Researchers frequently inquire about "analytical methods for CAS 89226-78-8" or "quality control of aminopyridine intermediates," underscoring the need for reliable quantification and impurity profiling. Proper storage conditions, typically under inert atmospheres and low temperatures, ensure long-term stability.

In summary, 3-(2-Aminopyridin-3-yl)propan-1-ol (CAS No. 89226-78-8) is a multifaceted compound with broad applications in life sciences and material engineering. Its relevance in drug discovery, agrochemicals, and synthetic chemistry makes it a subject of ongoing research and commercial interest. As industries prioritize innovation and sustainability, this compound is poised to play a pivotal role in future scientific breakthroughs.

• 954240-84-7(2-(2-aminopyridin-3-yl)ethan-1-ol)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)