Cas no 51953-13-0 (Pyrimidin-2-ol)
Pyrimidin-2-ol Chemical and Physical Properties
Names and Identifiers
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- Pyrimidin-2-ol
- 2-Pyrimidinol (7CI,9CI)
- 2-Hydroxypyrimidine
- 2-Pyrimidinol
- 2‐PYRIMIDINOL
- pyrimidone
- CS-0021072
- Pyrimidin-2(1H)-one
- A871112
- AM803987
- NSC-618280
- 1H-pyrimidinone
- 13K708ILY4
- 557-01-7
- AKOS000117994
- 2-pyrimidone
- A830762
- 2-Pyrimidinol #
- CHEMBL1650607
- AKOS016028433
- EN300-27696
- SY020185
- 2-pyrimidinone
- 71O
- 1,2-dihydropyrimidin-2-one
- (1H)-pyrimidinone
- 2-pyridiminol
- NS00043043
- 51953-13-0
- UNII-13K708ILY4
- NSC618280
- Pyridiminol
- W-203100
- 2(1H)-Pyrimidinone
- AC-15597
- FT-0751601
- AB-323/25048086
- BCP30399
- pyrimidin-2-one
- 55949-38-7
- 2-Pyrimidinol;
- 2-OXOPYRIMIDINE(HCl salt form)
- SB55522
- DTXSID4060315
- Q17572764
- 1H-Pyrimidin-2-one
- O10847
- 2-Oxopyrimidine
- MFCD00047358
- 2(1H)-PYRIMIDONE
- GS-6298
- CHEBI:53577
- EINECS 209-149-8
- FT-0604349
- DB-014121
- pyrimidine, 2-hydroxy-
- DA-05258
-
- MDL: MFCD00047358
- Inchi: 1S/C4H4N2O/c7-4-5-2-1-3-6-4/h1-3H,(H,5,6,7)
- InChI Key: VTGOHKSTWXHQJK-UHFFFAOYSA-N
- SMILES: O=C1N=CC=CN1
Computed Properties
- Exact Mass: 96.03242
- Monoisotopic Mass: 96.032363
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 7
- Rotatable Bond Count: 0
- Complexity: 137
- 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
- Surface Charge: 0
- Tautomer Count: 2
- XLogP3: nothing
- Topological Polar Surface Area: 41.5
Experimental Properties
- Color/Form: No data avaiable
- Density: 1.2604 (rough estimate)
- Melting Point: No data available
- Boiling Point: 179.58°C (rough estimate)
- Flash Point: 140.8°C
- Refractive Index: 1.4610 (estimate)
- PSA: 46.01
- Vapor Pressure: No data available
Pyrimidin-2-ol Security Information
- Signal Word:Warning
- Hazard Statement: H315 (100%) H319 (100%) H335 (100%)
-
Warning Statement:
P264Thoroughly clean after treatment
P280Wear protective gloves/Wear protective clothing/Wear protective goggles/Wear a protective mask
P305If it enters the eyes
P351Rinse carefully with water for a few minutes
P338Remove the contact lens(If any)And easy to operate,Continue flushing
P337If eye irritation persists
P313Obtain medical advice/care - Safety Instruction: H315 (100%) H319 (100%) H335 (100%)
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
Pyrimidin-2-ol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | P303873-250mg |
Pyrimidin-2-ol |
51953-13-0 | 95% | 250mg |
¥51.00 | 2021-05-25 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | P303873-1g |
Pyrimidin-2-ol |
51953-13-0 | 95% | 1g |
¥62.90 | 2023-09-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | P303873-5g |
Pyrimidin-2-ol |
51953-13-0 | 95% | 5g |
¥257.90 | 2023-09-01 | |
| Ambeed | A118857-1g |
Pyrimidin-2-ol |
51953-13-0 | 95+% | 1g |
$10.00 | 2021-07-07 | |
| Ambeed | A118857-5g |
Pyrimidin-2-ol |
51953-13-0 | 95+% | 5g |
$42.00 | 2021-07-07 | |
| Ambeed | A118857-10g |
Pyrimidin-2-ol |
51953-13-0 | 95+% | 10g |
$81.00 | 2021-07-07 | |
| Ambeed | A118857-25g |
Pyrimidin-2-ol |
51953-13-0 | 95+% | 25g |
$188.00 | 2021-07-07 | |
| Ambeed | A118857-100g |
Pyrimidin-2-ol |
51953-13-0 | 95+% | 100g |
$749.00 | 2021-07-07 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-PL225-20g |
Pyrimidin-2-ol |
51953-13-0 | 95+% | 20g |
¥1683.0 | 2022-06-09 | |
| Chemenu | CM165359-25g |
2-Pyrimidinol |
51953-13-0 | 95%+ | 25g |
$167 | 2024-07-15 |
Pyrimidin-2-ol Suppliers
Pyrimidin-2-ol Related Literature
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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
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Brindha J.,Balamurali M. M.,Kaushik Chanda RSC Adv., 2019,9, 34720-34734
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Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
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Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
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Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
Additional information on Pyrimidin-2-ol
Pyrimidin-2-ol (CAS No. 51953-13-0): A Key Intermediate in Modern Pharmaceutical and Chemical Research
Pyrimidin-2-ol, chemically known by its CAS number 51953-13-0, is a significant compound in the realm of pharmaceutical and chemical synthesis. This heterocyclic organic compound belongs to the pyrimidine family, a class of molecules widely recognized for their diverse biological activities and applications in medicinal chemistry. The structural simplicity of Pyrimidin-2-ol, featuring a pyrimidine ring substituted with a hydroxyl group at the 2-position, makes it a versatile intermediate in the synthesis of various pharmacologically active agents.
The utility of Pyrimidin-2-ol extends across multiple domains of chemical research, particularly in the development of new drugs and agrochemicals. Its unique structural framework allows for facile functionalization at multiple sites, enabling chemists to tailor its properties for specific applications. In recent years, the demand for Pyrimidin-2-ol has surged due to its role as a precursor in the synthesis of nucleoside analogs, which are crucial in antiviral and anticancer therapies.
One of the most compelling aspects of Pyrimidin-2-ol is its incorporation into nucleoside-based drugs. Nucleoside analogs mimic the natural nucleosides found in DNA and RNA but are structurally modified to interfere with viral replication or cancer cell proliferation. Pyrimidin-2-ol serves as a foundational building block for these analogs, allowing researchers to design molecules that can selectively inhibit specific enzymes or pathways involved in disease processes. For instance, derivatives of Pyrimidin-2-ol have been explored as potential inhibitors of polymerases, enzymes essential for viral genome replication.
Recent advancements in synthetic methodologies have further enhanced the accessibility and efficiency of Pyrimidin-2-ol production. Modern techniques such as catalytic hydrogenation and palladium-catalyzed cross-coupling reactions have enabled the scalable synthesis of Pyrimidin-2-ol with high purity and yield. These improvements have not only reduced costs but also opened new avenues for drug discovery programs that rely on this compound.
The pharmaceutical industry has taken particular interest in Pyrimidin-2-ol due to its potential in developing treatments for a range of diseases. Researchers are currently investigating its derivatives as candidates for antiviral drugs, particularly against emerging viruses that pose significant public health challenges. Additionally, Pyrimidin-2-ol-based compounds are being studied for their anti-inflammatory properties, making them promising candidates for treating chronic inflammatory diseases such as rheumatoid arthritis.
Beyond pharmaceutical applications, Pyrimidin-2-ol finds utility in agrochemical research. Its structural motifs are incorporated into herbicides and fungicides that target specific enzymatic pathways in pests and weeds. By leveraging the reactivity of the hydroxyl group and the pyrimidine core, chemists can design molecules that exhibit high selectivity and low toxicity to non-target organisms.
The chemical properties of Pyrimidin-2-ol also make it an attractive candidate for material science applications. Its ability to form stable complexes with metals and other small molecules has led to investigations into its use as a ligand in catalysis or as a component in functional materials such as organic semiconductors.
In conclusion, Pyrimidin-2-ol (CAS No. 51953-13-0) is a multifaceted compound with broad applications across pharmaceuticals, agrochemicals, and materials science. Its role as a key intermediate in synthesizing biologically active molecules underscores its importance in modern chemical research. As synthetic methodologies continue to evolve, the potential uses for Pyrimidin-2-ol are likely to expand, driving further innovation and discovery.
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