1-三苯甲基-3-溴-5-叠氮基吲唑
5-Azido-3-iodo-1-trityl-1H-indazole
CAS: 1403667-60-6
Molecular Formula: C26H18IN5
1-三苯甲基-3-溴-5-叠氮基吲唑 - Names and Identifiers
| Name | 5-Azido-3-iodo-1-trityl-1H-indazole |
| Synonyms | 5-Azido-3-iodo-1-trityl-1H-indazole 5-azido-3-iodo-1-trityl-1H-indazole 1H-Indazole, 5-azido-3-iodo-1-trityl- |
| CAS | 1403667-60-6 |
1-三苯甲基-3-溴-5-叠氮基吲唑 - Physico-chemical Properties
| Molecular Formula | C26H18IN5 |
| Molar Mass | 527.37 |
1-三苯甲基-3-溴-5-叠氮基吲唑 - Introduction
1-Trityl-3-bromo-5-azidoindazole (abbreviated BTZ) is an organic compound. Here are some of its properties, uses, manufacturing and safety information.
Nature:
-Appearance: White solid.
-Solubility: Soluble in organic solvents such as chloroform, acetone and methanol.
-Thermal stability: stable at room temperature, but may decompose at high temperature.
Use:
-As a catalyst: BTZ can be used as a catalyst to catalyze organic synthesis reactions, such as electrophilic substitution reactions, hydroxylation reactions, etc.
-As a fluorescent probe: BTZ has the structure of grass ketone, which can be used for fluorescence sensitive detection, such as the detection of metal ions, the detection of environmental pollutants, etc.
-Other applications: BTZ can also be used as an intermediate or ligand in organic synthesis.
Preparation Method:
BTZ is usually synthesized by chemical reaction, and its preparation method is complicated. A common method is to react triphenyl ketone with trityl bromide to obtain trityl iodide ketone, which then undergoes a series of reactions to produce BTZ.
Safety Information:
- BTZ is an organic compound and should be used with caution to avoid direct contact with skin, eyes and respiratory tract.
-Personal protective equipment such as lab gloves, goggles and protective masks should be used during operation.
-Avoid inhaling its dust or vapor, and should operate under well-ventilated laboratory conditions.
-When disposing of or disposing of waste, follow local chemical waste disposal regulations.
Please note that since BTZ is a professional compound, it is necessary to fully understand and master the corresponding safety operation knowledge when operating, and comply with the relevant safety operation procedures.
Nature:
-Appearance: White solid.
-Solubility: Soluble in organic solvents such as chloroform, acetone and methanol.
-Thermal stability: stable at room temperature, but may decompose at high temperature.
Use:
-As a catalyst: BTZ can be used as a catalyst to catalyze organic synthesis reactions, such as electrophilic substitution reactions, hydroxylation reactions, etc.
-As a fluorescent probe: BTZ has the structure of grass ketone, which can be used for fluorescence sensitive detection, such as the detection of metal ions, the detection of environmental pollutants, etc.
-Other applications: BTZ can also be used as an intermediate or ligand in organic synthesis.
Preparation Method:
BTZ is usually synthesized by chemical reaction, and its preparation method is complicated. A common method is to react triphenyl ketone with trityl bromide to obtain trityl iodide ketone, which then undergoes a series of reactions to produce BTZ.
Safety Information:
- BTZ is an organic compound and should be used with caution to avoid direct contact with skin, eyes and respiratory tract.
-Personal protective equipment such as lab gloves, goggles and protective masks should be used during operation.
-Avoid inhaling its dust or vapor, and should operate under well-ventilated laboratory conditions.
-When disposing of or disposing of waste, follow local chemical waste disposal regulations.
Please note that since BTZ is a professional compound, it is necessary to fully understand and master the corresponding safety operation knowledge when operating, and comply with the relevant safety operation procedures.
Last Update：2024-04-09 15:17:52
