2,5-Furandione, dihydro-3-(tetrapropenyl)-, reaction products with triethanolamine
2,5-Furandione, dihydro-3-(tetrapropenyl)-, reaction products with triethanolamine
CAS: 68877-10-1
Molecular Formula: C22H35NO6
2,5-Furandione, dihydro-3-(tetrapropenyl)-, reaction products with triethanolamine - Names and Identifiers
2,5-Furandione, dihydro-3-(tetrapropenyl)-, reaction products with triethanolamine - Physico-chemical Properties
| Molecular Formula | C22H35NO6 |
| Molar Mass | 409.5164 |
2,5-Furandione, dihydro-3-(tetrapropenyl)-, reaction products with triethanolamine - Introduction
Dihydro-3-tetrapropenyl-2, 5-furanedione is an organic compound, also known as ketoaldehyde. It reacts with triethanolamine to produce a product called Schiff base. The following is a description of the properties, uses, preparation and safety information of Schiff bases:
Nature:
Schiff bases are organic compounds, usually yellow or orange solids. It has good stability in solution. Schiff bases contain nitrogen atoms in their molecules and can form complexes with many metal ions through coordination.
Use:
Schiff bases have a wide range of applications in chemistry and biology. They are commonly used as dyes, catalysts and ligands. In organic synthesis, Schiff bases have the ability to catalyze acid-base reactions, redox reactions, oxidative coupling reactions and other reactions. In addition, Schiff bases can also be used for the detection of metal ions and the preparation of fluorescent probes.
Method:
dihydro-3-tetrapropenyl -2,5-furanedione reacts with triethanolamine to produce Schiff base. Generally, the preparation method is to mix the two compounds in an appropriate solvent and heat the reaction. In general, the reaction solution is heated to reflux temperature and the reaction is continued for a period of time, followed by cooling, crystallization or purification by distillation to obtain the product.
Safety Information:
When handling Schiff base, take care to avoid inhaling its dust, liquid or vapor. Wear protective glasses and gloves to ensure good ventilation in the laboratory. If contact with skin or eyes, rinse immediately with water and seek medical help. In addition, Schiff base should also be stored in a sealed container and away from combustibles and oxidants.
Nature:
Schiff bases are organic compounds, usually yellow or orange solids. It has good stability in solution. Schiff bases contain nitrogen atoms in their molecules and can form complexes with many metal ions through coordination.
Use:
Schiff bases have a wide range of applications in chemistry and biology. They are commonly used as dyes, catalysts and ligands. In organic synthesis, Schiff bases have the ability to catalyze acid-base reactions, redox reactions, oxidative coupling reactions and other reactions. In addition, Schiff bases can also be used for the detection of metal ions and the preparation of fluorescent probes.
Method:
dihydro-3-tetrapropenyl -2,5-furanedione reacts with triethanolamine to produce Schiff base. Generally, the preparation method is to mix the two compounds in an appropriate solvent and heat the reaction. In general, the reaction solution is heated to reflux temperature and the reaction is continued for a period of time, followed by cooling, crystallization or purification by distillation to obtain the product.
Safety Information:
When handling Schiff base, take care to avoid inhaling its dust, liquid or vapor. Wear protective glasses and gloves to ensure good ventilation in the laboratory. If contact with skin or eyes, rinse immediately with water and seek medical help. In addition, Schiff base should also be stored in a sealed container and away from combustibles and oxidants.
Last Update：2024-04-09 20:52:54
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