1133057-97-2
[9-(1-naphthalenyl)-9H-carbazol-3-yl]-Boronic acid
CAS: 1133057-97-2
Molecular Formula: C22H16BNO2
1133057-97-2 - Names and Identifiers
1133057-97-2 - Physico-chemical Properties
| Molecular Formula | C22H16BNO2 |
| Molar Mass | 337.18 |
| Density | 1.22±0.1 g/cm3 (20 ºC 760 Torr) |
| Boling Point | 548.4±56.0 °C(Predicted) |
| pKa | 8.82±0.30(Predicted) |
1133057-97-2 - Introduction
N-(1-naphthyl) carbazole boronic acid is an organic compound having the following properties and uses.
Nature:
-Appearance as a white crystalline solid.
-Stable at room temperature.
-has strong fluorescence properties, can emit yellow green fluorescence.
Use:
-Often used as an intermediate in the synthesis of fluorescent dyes.
-Can be used to prepare optoelectronic devices, organic semiconductor materials, etc.
Preparation Method:
The preparation of N-(1-naphthyl) carbazole boronic acid is usually completed by the following steps:
1. first synthesis of 1-naphthalene methanol and halogenated hydrocarbon reaction to obtain N-(1-naphthyl) halogenated hydrocarbon compounds.
2. The obtained N-(1-naphthyl) halogenated hydrocarbon is reacted with carbazole boronic acid to produce N-(1-naphthyl) carbazole boronic acid.
Safety Information:
- N-(1-naphthyl) carbazole boronic acid is stable at room temperature, but long-term contact with skin and inhalation of its powder should be avoided.
-Wear appropriate protective gloves, glasses and masks during operation.
-Wash immediately or seek medical help if exposed or inhaled.
Please note that when conducting chemical research and experiments, strictly abide by safe operations and regulations to ensure laboratory safety.
Nature:
-Appearance as a white crystalline solid.
-Stable at room temperature.
-has strong fluorescence properties, can emit yellow green fluorescence.
Use:
-Often used as an intermediate in the synthesis of fluorescent dyes.
-Can be used to prepare optoelectronic devices, organic semiconductor materials, etc.
Preparation Method:
The preparation of N-(1-naphthyl) carbazole boronic acid is usually completed by the following steps:
1. first synthesis of 1-naphthalene methanol and halogenated hydrocarbon reaction to obtain N-(1-naphthyl) halogenated hydrocarbon compounds.
2. The obtained N-(1-naphthyl) halogenated hydrocarbon is reacted with carbazole boronic acid to produce N-(1-naphthyl) carbazole boronic acid.
Safety Information:
- N-(1-naphthyl) carbazole boronic acid is stable at room temperature, but long-term contact with skin and inhalation of its powder should be avoided.
-Wear appropriate protective gloves, glasses and masks during operation.
-Wash immediately or seek medical help if exposed or inhaled.
Please note that when conducting chemical research and experiments, strictly abide by safe operations and regulations to ensure laboratory safety.
Last Update：2024-04-09 15:17:51
