9-Ethyl-9H-carbazole-3-carboxaldehyde - Names and Identifiers
9-Ethyl-9H-carbazole-3-carboxaldehyde - Physico-chemical Properties
Molecular Formula | C15H13NO
|
Molar Mass | 223.27 |
Density | 1.0707 (rough estimate) |
Melting Point | 85-87 °C (lit.) |
Boling Point | 255 °C / 15mmHg |
Flash Point | 163.5°C |
Solubility | soluble in Benzene,Toluene |
Vapor Presure | 5.66E-05mmHg at 25°C |
Appearance | Crystalline Powder or Granules |
Color | Yellow to ochre |
Storage Condition | 2-8°C |
Refractive Index | 1.5500 (estimate) |
MDL | MFCD00004963 |
Physical and Chemical Properties | White crystalline powder. Melting point 85-87 °c. |
9-Ethyl-9H-carbazole-3-carboxaldehyde - Risk and Safety
Risk Codes | R22 - Harmful if swallowed
R36 - Irritating to the eyes
|
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
|
WGK Germany | 3 |
HS Code | 29339900 |
9-Ethyl-9H-carbazole-3-carboxaldehyde - Introduction
N-Ethyl-3-carbazolecarboxaldehyde is an organic compound whose chemical formula is C14H13NO. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: N-Ethyl-3-carbazolecarboxaldehyde is a light yellow to dark orange crystal or oily liquid.
-Solubility: It can be dissolved in common organic solvents, such as ethanol, dimethylformamide and dichloromethane.
-Melting point: The melting point of the N-Ethyl-3-carbazolecarboxaldehyde is between 40-45°C.
Use:
N-Ethyl-3-carbazolecarboxaldehyde has important applications in the field of organic synthesis, including:
-Fluorescent probe: It can be used as a fluorescent probe for biological detection and analysis.
-Photosensitizer: It can be used as a photosensitizer for dye-sensitized solar cells.
-Others: In addition, it is also used in some important reactions in organic synthesis, such as oxidation, reduction and cyclization reactions.
Preparation Method:
The method for preparing N-Ethyl-3-carbazolecarboxaldehyde can be obtained by reacting carbazole with N-ethylformamide, and then performing a hydroformylation reaction with an acid catalyst.
Safety Information:
- N-Ethyl-3-carbazolecarboxaldehyde toxicity information is limited, but due to its organic nature, appropriate safety measures should be taken.
-Appropriate protective equipment, such as lab gloves and goggles, must be worn when using or handling the compound.
-Avoid contact with skin, eyes and clothing, and keep the work area well ventilated.
-If swallowing or inhalation occurs, seek medical attention immediately.
Last Update:2024-04-10 22:29:15