1,3,5-Trifluoro-2,4,6-triiodobenzene - Names and Identifiers
Name | 1,3,5-Trifluoro-2,4,6-triiodobenzene
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Synonyms | 1,3,5-Trifluoro-2,4 1,3,5-Trifluoro-2,4,6-Triiodob 1,3,5-Trifluoro-2,4,6-triiodobenzene 1,3,5-TRIFLUORO-2,4,6-TRIIODOBENZENE 1,3,5-TRILFLUORO-2,4,6-TRIIODOBENZENE Benzene,1,3,5-trifluoro-2,4,6-triiodo- benzene, 1,3,5-trifluoro-2,4,6-triiodo-
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CAS | 84322-56-5
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InChI | InChI=1/C6F3I3/c7-1-4(10)2(8)6(12)3(9)5(1)11 |
1,3,5-Trifluoro-2,4,6-triiodobenzene - Physico-chemical Properties
Molecular Formula | C6F3I3
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Molar Mass | 509.77 |
Density | 3.029±0.06 g/cm3(Predicted) |
Melting Point | 152℃ |
Boling Point | 352.4±37.0 °C(Predicted) |
Flash Point | 148.5°C |
Water Solubility | Slightly soluble in water. |
Vapor Presure | 7.82E-05mmHg at 25°C |
Storage Condition | 2-8°C(protect from light) |
Sensitive | Light Sensitive |
Refractive Index | 1.698 |
1,3,5-Trifluoro-2,4,6-triiodobenzene - Risk and Safety
Hazard Symbols | Xi - Irritant
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Hazard Class | IRRITANT |
1,3,5-Trifluoro-2,4,6-triiodobenzene - Introduction
1,3,5-Trifluoro-2,4,6-triiodobenzene is an organic compound with the formula C6F3I3, which has the following properties:
1. Physical properties: 1,3,5-Trifluoro-2,4,6-triiodobenzene is a yellow crystal with a high melting point and boiling point. Solid at room temperature, soluble in organic solvents such as ethers and ketones, insoluble in water.
2. Chemical properties: The special structure of the compound makes it have certain chemical activity. It can be used as a reagent to participate in substitution reactions in organic synthesis and reactions.
3. Application: 1,3,5-Trifluoro-2,4,6-triiodobenzene has certain application value in the field of organic chemistry. It can be used as a reagent to participate in the substitution reactions of carbon-fluorine bonds and carbon-iodine bonds in organic reactions. In addition, it can also be used to study synthesis in fields such as material science and medicinal chemistry.
4. Preparation method: The preparation method of 1,3,5-Trifluoro-2,4,6-triiodobenzene is mainly achieved by substitution reaction. The common method is to prepare 2,4, 6-triiodobenzene first, and then carry out fluorination reaction under appropriate conditions to replace part of the iodine atoms of triiodobenzene with fluorine atoms.
5. Safety information: Since 1,3,5-Trifluoro-2,4,6-triiodobenzene is an organic compound, attention should be paid to its safety during use and storage. It may have irritating and harmful effects on the human body, so you should wear appropriate protective equipment and follow relevant safety procedures when operating. In addition, it may also cause pollution to the environment, and attention should be paid to prevent its leakage and discharge.
Last Update:2024-04-09 21:04:16