Cas no 1227574-72-2 ((5-Fluoropyrimidin-2-yl)methanol)
(5-Fluoropyrimidin-2-yl)methanol Chemical and Physical Properties
Names and Identifiers
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- (5-Fluoropyrimidin-2-yl)methanol
- 5-Fluoropyrimidine-2-methanol
- DS-000084
- AKOS025243838
- PB28593
- EN300-261484
- 5-FLUORO-2-(HYDROXYMETHYL)PYRIMIDINE
- SY036740
- P11889
- F2147-5288
- DTXSID00856620
- CS-0053146
- MFCD16611296
- AS-51088
- 1227574-72-2
- 2-Pyrimidinemethanol, 5-fluoro-
- CZB57472
-
- MDL: MFCD16611296
- Inchi: 1S/C5H5FN2O/c6-4-1-7-5(3-9)8-2-4/h1-2,9H,3H2
- InChI Key: TXZSJRMEHFCYPZ-UHFFFAOYSA-N
- SMILES: FC1C=NC(CO)=NC=1
Computed Properties
- Exact Mass: 128.03859095g/mol
- Monoisotopic Mass: 128.03859095g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 9
- Rotatable Bond Count: 1
- Complexity: 83
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: -0.5
- Topological Polar Surface Area: 46?2
Experimental Properties
- Density: 1.364±0.06 g/cm3 (20 oC 760 Torr),
- Boiling Point: 200.3±20.0 oC (760 Torr),
- Flash Point: 74.9±21.8 oC,
- Solubility: Soluble (143 g/l) (25 o C),
(5-Fluoropyrimidin-2-yl)methanol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Matrix Scientific | 122462-1g |
5-Fluoropyrimidine-2-methanol, 97.0% |
1227574-72-2 | 97.0% | 1g |
$1552.00 | 2023-09-06 | |
| TRC | B435150-10mg |
(5-Fluoropyrimidin-2-yl)methanol |
1227574-72-2 | 10mg |
$ 50.00 | 2022-06-07 | ||
| TRC | B435150-50mg |
(5-Fluoropyrimidin-2-yl)methanol |
1227574-72-2 | 50mg |
$ 65.00 | 2022-06-07 | ||
| TRC | B435150-100mg |
(5-Fluoropyrimidin-2-yl)methanol |
1227574-72-2 | 100mg |
$ 80.00 | 2022-06-07 | ||
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | F172724-250mg |
(5-Fluoropyrimidin-2-yl)methanol |
1227574-72-2 | 97% | 250mg |
¥2221.90 | 2023-09-02 | |
| Alichem | A039001992-250mg |
5-Fluoropyrimidine-2-methanol |
1227574-72-2 | 95% | 250mg |
$444.97 | 2023-09-03 | |
| Alichem | A039001992-1g |
5-Fluoropyrimidine-2-methanol |
1227574-72-2 | 95% | 1g |
$1037.50 | 2023-09-03 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBN2011200-250 MG |
(5-fluoropyrimidin-2-yl)methanol |
1227574-72-2 | 97% | 250MG |
¥ 1,386.00 | 2021-05-07 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBN2011200-500 MG |
(5-fluoropyrimidin-2-yl)methanol |
1227574-72-2 | 97% | 500MG |
¥ 2,772.00 | 2021-05-07 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBN2011200-1 G |
(5-fluoropyrimidin-2-yl)methanol |
1227574-72-2 | 97% | 1g |
¥ 4,158.00 | 2021-05-07 |
(5-Fluoropyrimidin-2-yl)methanol Suppliers
(5-Fluoropyrimidin-2-yl)methanol Related Literature
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Raktani Bikshapathi,Sai Prathima Parvathaneni,Vaidya Jayathirtha Rao Green Chem., 2017,19, 4446-4450
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Andre Prates Pereira,Tao Dong,Eric P. Knoshaug,Nick Nagle,Ryan Spiller,Bonnie Panczak,Christopher J. Chuck,Philip T. Pienkos Sustainable Energy Fuels, 2020,4, 3400-3408
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Jialiang Yuan,Ran Dong,Yuan Li,Yang Liu,Zhuo Zheng,Yuxia Liu,Yan Sun,Benhe Zhong,Zhenguo Wu,Xiaodong Guo Chem. Commun., 2021,57, 13004-13007
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Piotr Szcze?niak,Sebastian Stecko RSC Adv., 2015,5, 30882-30888
Additional information on (5-Fluoropyrimidin-2-yl)methanol
Comprehensive Guide to (5-Fluoropyrimidin-2-yl)methanol (CAS No. 1227574-72-2): Properties, Applications, and Market Insights
(5-Fluoropyrimidin-2-yl)methanol (CAS No. 1227574-72-2) is a fluorinated pyrimidine derivative that has garnered significant attention in pharmaceutical and agrochemical research. This compound, characterized by its unique fluoropyrimidine core and hydroxymethyl functional group, serves as a versatile building block in organic synthesis. Its molecular formula, C5H5FN2O, and molecular weight of 128.10 g/mol make it a valuable intermediate for designing novel bioactive molecules.
The 5-fluoropyrimidine scaffold is widely recognized for its role in medicinal chemistry, particularly in the development of antiviral and anticancer agents. Researchers are increasingly exploring (5-Fluoropyrimidin-2-yl)methanol as a precursor for nucleoside analogs, which are crucial in drug discovery programs targeting RNA viruses and cellular proliferation pathways. Recent studies highlight its potential in creating fluorinated pharmaceuticals with enhanced metabolic stability and bioavailability.
In agrochemical applications, (5-Fluoropyrimidin-2-yl)methanol derivatives have shown promise as crop protection agents. The introduction of fluorine atoms into pyrimidine structures often improves their pesticidal activity and environmental persistence. This aligns with the growing demand for sustainable agrochemicals that address global food security challenges while minimizing ecological impact.
The synthesis of (5-Fluoropyrimidin-2-yl)methanol typically involves fluorination reactions of pyrimidine precursors, followed by selective oxidation or reduction steps. Advanced purification techniques such as column chromatography and recrystallization ensure high purity (>98%), which is critical for research and industrial applications. Analytical characterization via NMR spectroscopy (1H, 13C, 1?F) and mass spectrometry confirms the structural integrity of this compound.
Market trends indicate rising demand for fluorinated building blocks like (5-Fluoropyrimidin-2-yl)methanol, driven by expanding pharmaceutical R&D budgets and the need for novel heterocyclic compounds. Suppliers are responding with improved manufacturing processes that enhance yield and reduce production costs. The compound's stability under standard storage conditions (2-8°C in inert atmosphere) makes it suitable for global distribution to research institutions and chemical enterprises.
From a regulatory perspective, (5-Fluoropyrimidin-2-yl)methanol is not classified as hazardous under current GHS criteria when handled with standard laboratory precautions. However, researchers should consult chemical safety data sheets (SDS) for proper handling procedures. The compound's environmental fate and toxicity profile are subjects of ongoing studies, particularly regarding its biodegradation pathways and ecotoxicological effects.
Emerging applications of (5-Fluoropyrimidin-2-yl)methanol include its use in material science, where fluorinated pyrimidines contribute to the development of specialty polymers with unique electronic properties. Additionally, its role in proteomics research as a potential labeling reagent for biomolecules is under investigation. These diverse applications underscore the compound's importance across multiple scientific disciplines.
For researchers sourcing (5-Fluoropyrimidin-2-yl)methanol, key considerations include supplier reliability, batch-to-batch consistency, and technical support for synthetic applications. Many manufacturers now provide custom synthesis services to meet specific research requirements, including isotopic labeling or structural modifications. The global market for this compound is projected to grow steadily, supported by increasing investments in precision medicine and green chemistry initiatives.
In conclusion, (5-Fluoropyrimidin-2-yl)methanol (CAS No. 1227574-72-2) represents a strategically important fluorinated heterocycle with broad utility in life sciences and materials research. Its unique chemical properties and synthetic versatility position it as a valuable tool for addressing contemporary challenges in drug discovery, sustainable agriculture, and advanced materials development.
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