Cas no 1803789-73-2 (2,4-Dimethyl-5-iodophenol)
2,4-Dimethyl-5-iodophenol Chemical and Physical Properties
Names and Identifiers
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- 2,4-Dimethyl-5-iodophenol
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- Inchi: 1S/C8H9IO/c1-5-3-6(2)8(10)4-7(5)9/h3-4,10H,1-2H3
- InChI Key: FJEXIDBVSJNLJU-UHFFFAOYSA-N
- SMILES: IC1C=C(C(C)=CC=1C)O
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 10
- Rotatable Bond Count: 0
- Complexity: 116
- XLogP3: 2.9
- Topological Polar Surface Area: 20.2
2,4-Dimethyl-5-iodophenol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A010009686-250mg |
2,4-Dimethyl-5-iodophenol |
1803789-73-2 | 97% | 250mg |
494.40 USD | 2021-07-06 | |
| Alichem | A010009686-500mg |
2,4-Dimethyl-5-iodophenol |
1803789-73-2 | 97% | 500mg |
806.85 USD | 2021-07-06 | |
| Alichem | A010009686-1g |
2,4-Dimethyl-5-iodophenol |
1803789-73-2 | 97% | 1g |
1,460.20 USD | 2021-07-06 |
2,4-Dimethyl-5-iodophenol Related Literature
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Xin Li,Liangliang Zhu,Sai Duan,Yanli Zhao,Hans ?gren Phys. Chem. Chem. Phys., 2014,16, 23854-23860
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Yuan-Jun Tong,Lu-Dan Yu,Lu-Lu Wu,Shu-Ping Cao,Ru-Ping Liang,Li Zhang,Xing-Hua Xia,Jian-Ding Qiu Chem. Commun., 2018,54, 7487-7490
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
Additional information on 2,4-Dimethyl-5-iodophenol
Comprehensive Guide to 2,4-Dimethyl-5-iodophenol (CAS No. 1803789-73-2): Properties, Applications, and Market Insights
2,4-Dimethyl-5-iodophenol (CAS No. 1803789-73-2) is a specialized organic compound that has garnered significant attention in the chemical and pharmaceutical industries. This iodinated phenol derivative is known for its unique structural properties, making it a valuable intermediate in synthetic chemistry. Researchers and manufacturers are increasingly interested in this compound due to its potential applications in drug development, agrochemicals, and material science.
The molecular structure of 2,4-Dimethyl-5-iodophenol features a phenol ring substituted with two methyl groups at the 2 and 4 positions and an iodine atom at the 5 position. This arrangement imparts distinct electronic and steric properties, which are crucial for its reactivity in various chemical reactions. The presence of the iodine atom makes it particularly useful in cross-coupling reactions, a hot topic in modern organic synthesis due to their efficiency in constructing complex molecules.
One of the most compelling aspects of 2,4-Dimethyl-5-iodophenol is its role in the synthesis of bioactive compounds. With the growing demand for novel pharmaceuticals, especially in areas like antimicrobial agents and anticancer drugs, this compound serves as a key building block. Its ability to undergo palladium-catalyzed reactions aligns with current trends in green chemistry, where researchers seek sustainable and efficient synthetic routes.
In addition to pharmaceuticals, 2,4-Dimethyl-5-iodophenol finds applications in the development of advanced materials. For instance, it can be used to modify polymers or create functionalized surfaces with specific properties. The compound's versatility is further highlighted by its potential use in organic electronics, a field that has seen exponential growth due to the rise of flexible and wearable technologies.
From a market perspective, the demand for 2,4-Dimethyl-5-iodophenol is expected to grow steadily. The increasing focus on precision medicine and tailored therapeutics has driven the need for high-quality chemical intermediates. Suppliers and manufacturers are investing in scalable synthesis methods to meet this demand while ensuring cost-effectiveness and environmental compliance.
For researchers working with 2,4-Dimethyl-5-iodophenol, handling and storage recommendations are critical. The compound should be stored in a cool, dry place, away from light and moisture, to maintain its stability. Proper safety measures, including the use of personal protective equipment (PPE), are essential when handling this chemical in the laboratory.
In summary, 2,4-Dimethyl-5-iodophenol (CAS No. 1803789-73-2) is a multifaceted compound with broad applications in pharmaceuticals, materials science, and beyond. Its unique properties and compatibility with modern synthetic techniques make it a valuable asset for researchers and industries alike. As scientific advancements continue to unfold, the relevance of this compound is poised to expand, offering new opportunities for innovation and discovery.
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