• 1. An approach to biodegradable star polymeric architectures using disulfide coupling?
  Jingquan Liu,Huiyun Liu,Zhongfan Jia,Volga Bulmus,Thomas P. Davis Chem. Commun., 2008, 6582-6584
• 2. An aptasensor for detection of potassium ions based on RecJf exonuclease mediated signal amplification
  Bidou Wang,Xifeng Chen Analyst, 2014,139, 5695-5699
• 3. An artificial blood vessel implanted three-dimensional microsystem for modeling transvascular migration of tumor cells?
  Xue-Ying Wang,Ying Pei,Min Xie,Zi-He Jin,Ya-Shi Xiao,Yang Wang,Li-Na Zhang,Yan Li,Wei-Hua Huang Lab Chip, 2015,15, 1178-1187
• 4. An intermolecular C–C coupling reaction of iridium complexes?
  Kathrin Kutlescha,Rhett Kempe New J. Chem., 2010,34, 1954-1960
• 5. An astrophysically-relevant mechanism for amino acid enantiomer enrichment
  Stephen P. Fletcher,Richard B. C. Jagt,Ben L. Feringa Chem. Commun., 2007, 2578-2580

Comprehensive Guide to (2-Cyclopropyloxazol-5-yl)methanol (CAS No. 1889959-79-8): Properties, Applications, and Market Insights

(2-Cyclopropyloxazol-5-yl)methanol (CAS No. 1889959-79-8) is a specialized heterocyclic compound that has garnered significant attention in pharmaceutical and agrochemical research. This compound, featuring a cyclopropyl-substituted oxazole core, is valued for its unique structural properties and potential applications in drug discovery. Researchers and industry professionals frequently search for "buy (2-Cyclopropyloxazol-5-yl)methanol" or "synthesis of 1889959-79-8," highlighting its growing relevance in synthetic chemistry.

The molecular structure of (2-Cyclopropyloxazol-5-yl)methanol combines a five-membered oxazole ring with a hydroxymethyl functional group, making it a versatile intermediate for further chemical modifications. Its CAS number 1889959-79-8 is often used in patent literature and regulatory documents, emphasizing its importance in intellectual property and compliance. Recent trends in "green chemistry" and "sustainable synthesis" have also increased interest in this compound due to its potential for eco-friendly production methods.

In pharmaceutical applications, (2-Cyclopropyloxazol-5-yl)methanol serves as a key building block for small-molecule drugs, particularly in oncology and infectious disease research. Its oxazole moiety is known to enhance bioavailability and metabolic stability, addressing common challenges in drug development. Searches like "1889959-79-8 biological activity" or "oxazole derivatives in medicine" reflect the scientific community's focus on its therapeutic potential.

The agrochemical industry also explores (2-Cyclopropyloxazol-5-yl)methanol for developing novel crop protection agents. Its structural features may contribute to pest resistance management, aligning with global demands for sustainable agriculture. Queries such as "CAS 1889959-79-8 for agrochemicals" or "cyclopropyloxazole uses" indicate its cross-industry appeal.

From a market perspective, the demand for high-purity (2-Cyclopropyloxazol-5-yl)methanol is rising, driven by advancements in custom synthesis and contract research organizations (CROs). Suppliers often list this compound under "rare chemical intermediates" or "pharma-grade building blocks," catering to niche markets. Analytical techniques like HPLC and NMR are critical for quality control, as emphasized in searches for "1889959-79-8 analytical data."

Innovations in catalysis and flow chemistry have improved the synthesis efficiency of (2-Cyclopropyloxazol-5-yl)methanol, reducing costs and environmental impact. Researchers investigating "scalable synthesis of oxazole derivatives" or "CAS 1889959-79-8 process optimization" will find this compound particularly relevant. Additionally, its stability under various conditions makes it suitable for long-term storage and global shipping.

Regulatory compliance is another critical aspect for CAS No. 1889959-79-8. While not classified as hazardous, proper handling guidelines are essential to ensure workplace safety. Documentation such as SDS (Safety Data Sheets) and COAs (Certificates of Analysis) are frequently requested by buyers, as seen in searches for "1889959-79-8 safety profile."

Future research on (2-Cyclopropyloxazol-5-yl)methanol may explore its role in bioconjugation or material science, expanding beyond traditional applications. The intersection of "AI-driven drug discovery" and "fragment-based screening" could further elevate its prominence. As a high-value chemical intermediate, this compound exemplifies the synergy between structural ingenuity and practical utility.

In summary, (2-Cyclopropyloxazol-5-yl)methanol (CAS No. 1889959-79-8) represents a compelling case study in modern chemical innovation. Its multifaceted applications, coupled with evolving synthetic methodologies, position it as a compound of enduring interest across scientific and industrial domains.

• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 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)
• 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)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)