Cas no 1806288-80-1 (2,5-Dichloro-4-(methylsulfonyl)pyrimidine)
2,5-Dichloro-4-(methylsulfonyl)pyrimidine Chemical and Physical Properties
Names and Identifiers
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- 2,5-Dichloro-4-(methylsulfonyl)pyrimidine
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- Inchi: 1S/C5H4Cl2N2O2S/c1-12(10,11)4-3(6)2-8-5(7)9-4/h2H,1H3
- InChI Key: XVMTUGKYQDPRBI-UHFFFAOYSA-N
- SMILES: ClC1=CN=C(N=C1S(C)(=O)=O)Cl
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 12
- Rotatable Bond Count: 1
- Complexity: 251
- XLogP3: 1.4
- Topological Polar Surface Area: 68.3
2,5-Dichloro-4-(methylsulfonyl)pyrimidine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A039002276-250mg |
2,5-Dichloro-4-(methylsulfonyl)pyrimidine |
1806288-80-1 | 98% | 250mg |
$890.43 | 2022-03-31 | |
| Alichem | A039002276-500mg |
2,5-Dichloro-4-(methylsulfonyl)pyrimidine |
1806288-80-1 | 98% | 500mg |
$1,271.49 | 2022-03-31 | |
| Alichem | A039002276-1g |
2,5-Dichloro-4-(methylsulfonyl)pyrimidine |
1806288-80-1 | 98% | 1g |
$1,983.77 | 2022-03-31 |
2,5-Dichloro-4-(methylsulfonyl)pyrimidine Related Literature
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
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Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
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Jason Wan Lab Chip, 2020,20, 4528-4538
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
Additional information on 2,5-Dichloro-4-(methylsulfonyl)pyrimidine
Comprehensive Overview of 2,5-Dichloro-4-(methylsulfonyl)pyrimidine (CAS No. 1806288-80-1)
2,5-Dichloro-4-(methylsulfonyl)pyrimidine (CAS No. 1806288-80-1) is a high-value pyrimidine derivative widely utilized in pharmaceutical and agrochemical research. This compound features a unique methylsulfonyl group, enhancing its reactivity and making it a critical intermediate in synthesizing advanced molecules. Its dichloropyrimidine backbone is particularly sought after for designing kinase inhibitors and antiviral agents, aligning with current trends in drug discovery targeting RNA-dependent RNA polymerase (RdRp) and tyrosine kinase pathways.
In recent years, the demand for sulfonyl-containing heterocycles like 2,5-Dichloro-4-(methylsulfonyl)pyrimidine has surged due to their role in developing small-molecule therapeutics. Researchers frequently search for "pyrimidine-based drug intermediates" or "methylsulfonyl pyrimidine applications," reflecting its relevance in cancer research and infectious disease studies. The compound’s electron-withdrawing properties also make it ideal for cross-coupling reactions, a hotspot in green chemistry and catalysis.
From a synthetic perspective, CAS 1806288-80-1 is pivotal for constructing N-heterocyclic scaffolds, a topic dominating medicinal chemistry forums. Its compatibility with Pd-catalyzed reactions and Suzuki-Miyaura couplings addresses frequent queries like "how to modify pyrimidine rings" or "best practices for sulfonyl group incorporation." These attributes position it as a versatile building block for high-throughput screening libraries.
Environmental and regulatory considerations further highlight the compound’s appeal. Unlike traditional halogenated reagents, 2,5-Dichloro-4-(methylsulfonyl)pyrimidine exhibits improved biodegradability profiles, resonating with sustainable chemistry initiatives. Searches for "eco-friendly sulfonyl precursors" or "low-toxicity pyrimidine synthesis" underscore its alignment with ESG (Environmental, Social, and Governance) goals in chemical manufacturing.
Analytical characterization of 1806288-80-1 typically involves HPLC purity assays and NMR spectroscopy, topics frequently explored in quality control discussions. The compound’s crystalline structure and solubility data are also critical for formulators, addressing common questions like "how to optimize pyrimidine solubility" or "stable sulfone derivatives for API development."
In summary, 2,5-Dichloro-4-(methylsulfonyl)pyrimidine (CAS No. 1806288-80-1) bridges multiple scientific disciplines, from drug design to material science. Its structural versatility and reaction efficiency ensure its prominence in peer-reviewed literature and industrial applications, making it a staple for researchers navigating next-generation therapeutic development.
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