2,4,5-TRIIODOIMIDAZOLE - Names and Identifiers
Name | 2,4,5-triiodo-1H-imidazole
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Synonyms | NSC 222411 BRN 0115451 2,4,5-TRIIODOIMIDAZOLE 2,4,5-Triiodoimidazole 2,4,5-triiodo-imidazol Imidazole, 2,4,5-triiodo- 2,4,5-TRIIODO-1H-IMIDAZOLE 2,4,5-triiodo-1H-imidazole 1H-Imidazole, 2,4,5-triiodo- 1H-Imidazole, 2,4,5-triiodo- (9CI) TIANFU CHEM--2,4,5-Triiodoimidazole
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CAS | 1746-25-4
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InChI | InChI=1/C3HI3N2/c4-1-2(5)8-3(6)7-1/h(H,7,8) |
2,4,5-TRIIODOIMIDAZOLE - Physico-chemical Properties
Molecular Formula | C3HI3N2
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Molar Mass | 445.77 |
Density | 3.504±0.06 g/cm3(Predicted) |
Melting Point | 188-190°C |
Boling Point | 459.2±50.0 °C(Predicted) |
Flash Point | 231.5°C |
Vapor Presure | 1.29E-08mmHg at 25°C |
pKa | 6.89±0.10(Predicted) |
Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
Refractive Index | 1.864 |
2,4,5-TRIIODOIMIDAZOLE - Risk and Safety
Hazard Symbols | Xn - Harmful
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Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin.
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Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
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UN IDs | UN 2811 6.1/PG III |
RTECS | NI8680000 |
Hazard Class | 6.1 |
Packing Group | III |
2,4,5-TRIIODOIMIDAZOLE - Introduction
2,4,5-triiodo-1H-imidazole is an organic compound with the chemical formula C6H2I3N3. The following is a description of the nature, use, preparation and safety information of 2,4,5-triiodo-1H-imidazole:
Nature:
-Appearance: 2,4,5-triiodo-1H-imidazole is colorless to light yellow crystal.
-Solubility: It is almost insoluble in water, but can be dissolved in some organic solvents, such as ethanol and dimethyl sulfoxide.
-Melting point: The melting point of 2,4,5-triiodo-1H-imidazole is 210-215°C.
-Chemical properties: It is an active iodine compound, which can be used as a reagent for substitution reactions and other organic synthesis reactions.
Use:
-Compound synthesis: 2,4,5-triiodo-1H-imidazole can be used as a reagent in organic synthesis and participate in various synthetic reactions, such as SUZUKI coupling reaction, synthesis of azoamine, etc.
-Biological activity: It is often used in the field of medicine to synthesize certain drugs, such as antibacterial agents and anti-cancer drugs.
Method:
- 2,4,5-triiodo-1H-imidazole is generally prepared by organic synthesis methods. A common method is to react an appropriate amount of imidazole with iodine to prepare its iodinated product.
Safety Information:
- 2,4,5-triiodo-1H-imidazole has certain chemical toxicity, such as accidental exposure or contact with eyes, skin, etc. may cause irritation and damage.
-During operation, care should be taken to wear appropriate protective equipment, such as gloves, goggles and laboratory coats.
-Avoid inhalation of dust and contact with skin. The affected area should be thoroughly cleaned after any contact.
-When storing, keep 2,4,5-triiodo-1H-imidazole in a sealed container, away from direct sunlight and high temperature environment.
-When using, storing and handling, please follow the relevant safety procedures.
Last Update:2024-04-09 02:00:43