9-Ethyl-3-formyl-9H-carbazole
N-Ethyl-3-carbazolecarboxaldehyde
CAS: 7570-45-8
Molecular Formula: C15H13NO
9-Ethyl-3-formyl-9H-carbazole - Names and Identifiers
| Name | N-Ethyl-3-carbazolecarboxaldehyde |
| Synonyms | N-ethyl-3-formylcarbazole N-ethylcarbazole-3-aldehyde 9-Ethyl-3-formyl-9H-carbazole N-ethylcarbazole-3-carbaldehyde N-Ethylcarbazole-3-carboxaldehye 9-ETHYLCARBAZOLE-3-CARBOXALDEHYDE N-Ethylcarbazole-3-carboxaldehyde N-Ethyl-3-carbazolecarboxaldehyde 9-ethyl-9H-carbazole-3-carbaldehyde 9-Ethyl-9H-carbazole-3-carboxaldehyde |
| CAS | 7570-45-8 |
| EINECS | 231-471-2 |
| InChI | InChI=1/C15H13NO/c1-2-16-14-6-4-3-5-12(14)13-9-11(10-17)7-8-15(13)16/h3-10H,2H2,1H3 |
9-Ethyl-3-formyl-9H-carbazole - 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-3-formyl-9H-carbazole - 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-3-formyl-9H-carbazole - 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.
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
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