• 1. Fe3O4 nanosphere@microporous organic networks: enhanced anode performances in lithium ion batteries through carbonization?
  Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
• 2. Evidence for the intrinsic nature of band-gap states electrochemically observed on atomically flat TiO2(110) surfaces?
  Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
• 3. Fe3O4/PEG-SO3H as a heterogeneous and magnetically-recyclable nanocatalyst for the oxidation of sulfides to sulfones or sulfoxides
  Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
• 4. Estimation of activation energy for electroporation and pore growth rate in liquid crystalline and gel phases of lipid bilayers using molecular dynamics simulations?
  Amit Kumar Majhi,Subbarao Kanchi,V. Venkataraman,K. G. Ayappa,Prabal K. Maiti Soft Matter, 2015,11, 8632-8640
• 5. Dissolution of cork biopolymers in biocompatible ionic liquids
  Helga Garcia,Rui Ferreira,Marija Petkovic,Jamie L. Ferguson,Maria C. Leit?o,H. Q. Nimal Gunaratne,Luís Paulo N. Rebelo Green Chem., 2010,12, 367-369

Comprehensive Overview of 1-(1,3-thiazol-2-yl)propan-1-ol (CAS No. 89464-29-9): Properties, Applications, and Industry Insights

1-(1,3-thiazol-2-yl)propan-1-ol (CAS No. 89464-29-9) is a specialized organic compound featuring a thiazole ring linked to a propanol moiety. This structural combination grants it unique physicochemical properties, making it valuable in pharmaceuticals, agrochemicals, and material science. The thiazole core, known for its electron-rich heterocyclic nature, enhances reactivity, while the hydroxyl group offers functional versatility. Researchers and industries are increasingly exploring its potential, particularly in drug intermediates and bioactive molecule synthesis.

In recent years, the demand for thiazole derivatives like 1-(1,3-thiazol-2-yl)propan-1-ol has surged due to their role in developing antimicrobial agents and anticancer compounds. A 2023 study highlighted its utility as a precursor for small-molecule inhibitors targeting enzyme pathways. This aligns with the growing focus on precision medicine and green chemistry, where efficient synthesis routes (e.g., catalytic hydrogenation) minimize waste. Users searching for "thiazole-based drug discovery" or "CAS 89464-29-9 applications" will find this compound relevant to cutting-edge research.

The compound's solubility in polar solvents (e.g., ethanol, DMSO) and stability under ambient conditions make it practical for lab-scale and industrial use. Analytical techniques like HPLC and NMR confirm its high purity (>98%), a critical factor for regulatory compliance in pharmaceutical manufacturing. Notably, its low toxicity profile (as per preliminary assays) positions it as a safer alternative to traditional halogenated intermediates, addressing sustainability concerns in chemical synthesis.

Emerging trends also link 1-(1,3-thiazol-2-yl)propan-1-ol to crop protection formulations. Its thiazole moiety disrupts fungal cell membranes, offering a template for next-generation fungicides. Agri-tech forums frequently discuss such derivatives under "eco-friendly pesticides," reflecting market shifts toward biodegradable solutions. Furthermore, patents filed between 2020–2024 highlight its incorporation into OLED materials, leveraging its electron-transport properties for flexible displays—a hotspot in material science innovations.

For suppliers and distributors, optimizing the supply chain of CAS No. 89464-29-9 requires adherence to REACH and GMP standards. Searches for "buy 1-(1,3-thiazol-2-yl)propan-1-ol" often prioritize vendors with ISO certification, underscoring quality expectations. Storage recommendations (e.g., inert atmosphere, 2–8°C) and MSDS documentation are equally critical to ensure safety and longevity, topics frequently queried in chemical procurement platforms.

In conclusion, 1-(1,3-thiazol-2-yl)propan-1-ol exemplifies the intersection of multidisciplinary chemistry and industrial demand. Its adaptability across life sciences and advanced materials sectors, coupled with stringent regulatory frameworks, ensures sustained relevance. Future research may explore its catalytic applications or polymeric composites, further expanding its commercial and scientific footprint.

• 40982-30-7(1-Thiazol-2-yl-ethanol)
• 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)