2-(2-naphthalenyl)-1H-indole
2-(2-naphthyl)-1H-indole
CAS: 23746-81-8
Molecular Formula: C18H13N
2-(2-naphthalenyl)-1H-indole - Names and Identifiers
| Name | 2-(2-naphthyl)-1H-indole |
| Synonyms | 2-(2-Naphthyl)indole 2-(2-NAPHTHYL)INDOLE 2-(2-naphthyl)-1H-indole 2-(2-Indolyl)naphthalene 2-(Naphth-2-yl)-1H-indole 2-(naphth-2-yl)-1h-indole 2-naphthalen-2-yl-1H-indole 2-(1H-Indol-2-yl)naphthalene 2-(2-naphthalenyl)-1H-indole 2-(naphthalen-2-yl)-1H-indole |
| CAS | 23746-81-8 |
| InChI | InChI=1/C18H13N/c1-2-6-14-11-16(10-9-13(14)5-1)18-12-15-7-3-4-8-17(15)19-18/h1-12,19H |
2-(2-naphthalenyl)-1H-indole - Physico-chemical Properties
| Molecular Formula | C18H13N |
| Molar Mass | 243.3 |
| Density | 1.208±0.06 g/cm3(Predicted) |
| Melting Point | 204-207°C |
| Boling Point | 469.5±14.0 °C(Predicted) |
| Flash Point | 211.3°C |
| Solubility | Soluble in DMSO. |
| Vapor Presure | 1.55E-08mmHg at 25°C |
| Appearance | powder to crystal |
| Color | Light yellow to Yellow to Green |
| pKa | 16.73±0.30(Predicted) |
| Storage Condition | 2-8℃ |
| Refractive Index | 1.737 |
| MDL | MFCD00124144 |
2-(2-naphthalenyl)-1H-indole - Risk and Safety
| Hazard Symbols | Xi - Irritant |
2-(2-naphthalenyl)-1H-indole - Introduction
2-(2-napthyl)-1H-indole is a kind of indole compound containing naphthalene group. Its chemical structure contains an indole ring and a naphthyl group attached to the indole nitrogen atom. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: 2-(2-napthyl)-1H-indole is a solid, the common form is white to yellow crystals.
-Melting point: Its melting point range is usually between 250-260 degrees Celsius.
-Solubility: It has certain solubility in common organic solvents, such as chloroform, dichloromethane and ethanol.
-Optical Properties: 2-(2-napthyl)-1H-indole has the ability to absorb and emit fluorescence in the ultraviolet region, making it useful in the fields of fluorescent probes and dyes.
Use:
-Fluorescent probe: Due to its fluorescent properties, it can be used as a fluorescent probe in the fields of chemical analysis, biomedical research and drug screening.
-Dye: 2-(2-napthyl)-1H-indole can also be used as an organic dye in the fields of dye-sensitized solar cells, laser dyes and fluorescent display devices.
Method:
- 2-(2-napthyl)-1H-indole is usually prepared by organic chemical synthesis methods. A common preparation method is to react 2-indoleamine with 2-naphthoate to produce a derivative of 2-(2-napthyl)-1H-indole, and then deprotect the derivative, the target product is obtained.
Safety Information:
- 2-(2-napthyl)-1H-indole has limited safety information, so general laboratory safety procedures should be followed when using or handling.
-It may cause potential harm to the environment, so it should be avoided in large quantities into water or soil.
-During processing, care should be taken to avoid direct contact with skin and eyes.
-Because its chemical structure contains a naphthyl group, it may have a potential impact on human health, so appropriate protective measures should be taken when operating, such as wearing gloves and protective glasses.
Nature:
-Appearance: 2-(2-napthyl)-1H-indole is a solid, the common form is white to yellow crystals.
-Melting point: Its melting point range is usually between 250-260 degrees Celsius.
-Solubility: It has certain solubility in common organic solvents, such as chloroform, dichloromethane and ethanol.
-Optical Properties: 2-(2-napthyl)-1H-indole has the ability to absorb and emit fluorescence in the ultraviolet region, making it useful in the fields of fluorescent probes and dyes.
Use:
-Fluorescent probe: Due to its fluorescent properties, it can be used as a fluorescent probe in the fields of chemical analysis, biomedical research and drug screening.
-Dye: 2-(2-napthyl)-1H-indole can also be used as an organic dye in the fields of dye-sensitized solar cells, laser dyes and fluorescent display devices.
Method:
- 2-(2-napthyl)-1H-indole is usually prepared by organic chemical synthesis methods. A common preparation method is to react 2-indoleamine with 2-naphthoate to produce a derivative of 2-(2-napthyl)-1H-indole, and then deprotect the derivative, the target product is obtained.
Safety Information:
- 2-(2-napthyl)-1H-indole has limited safety information, so general laboratory safety procedures should be followed when using or handling.
-It may cause potential harm to the environment, so it should be avoided in large quantities into water or soil.
-During processing, care should be taken to avoid direct contact with skin and eyes.
-Because its chemical structure contains a naphthyl group, it may have a potential impact on human health, so appropriate protective measures should be taken when operating, such as wearing gloves and protective glasses.
Last Update：2024-04-09 21:04:16
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