124337-34-4
9-(1H-benzotriazol-1-ylmethyl)-9H-carbazole
CAS: 124337-34-4
Molecular Formula: C19H14N4
124337-34-4 - Names and Identifiers
| Name | 9-(1H-benzotriazol-1-ylmethyl)-9H-carbazole |
| Synonyms | Benzotriazolylmetylcarbazole 9-(1H-Benzotriazol-1-ylmetyl)-9H-carbazole 9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole 9-(1H-benzotriazol-1-ylmethyl)-9H-carbazole 9-(1H-BENZOTRIAZOL-1-YLMETHYL)-9H-CARBAZOLE 9-[(1H-Benzotriazole-1-yl)methyl]-9H-carbazole 9-((1H-benzo[d][1,2,3]triazol-1-yl)methyl)-9H-carbazole |
| CAS | 124337-34-4 |
| InChI | InChI=1/C19H14N4/c1-4-10-17-14(7-1)15-8-2-5-11-18(15)22(17)13-23-19-12-6-3-9-16(19)20-21-23/h1-12H,13H2 |
124337-34-4 - Physico-chemical Properties
| Molecular Formula | C19H14N4 |
| Molar Mass | 298.34 |
| Density | 1.31g/cm3 |
| Melting Point | 190-193 °C (lit.) |
| Boling Point | 479.8°C at 760 mmHg |
| Flash Point | 243.9°C |
| Vapor Presure | 2.3E-09mmHg at 25°C |
| Appearance | powder to crystal |
| Color | White to Light yellow to Light orange |
| Storage Condition | 2-8℃ |
| Refractive Index | 1.738 |
| MDL | MFCD00216631 |
124337-34-4 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| 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 |
124337-34-4 - Introduction
9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole is an organic compound with the chemical formula C10H8N4. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: 9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole is a white crystalline solid.
-Melting point: Its melting point range is 235-240 degrees Celsius.
-Solubility: 9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole is soluble in some organic solvents.
Use:
9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole has a variety of uses in chemical research and industrial production, including:
-As an intermediate in organic synthesis, it can be used to synthesize other organic compounds.
-In the field of medicine, it can be used as a raw material for certain drugs and has biological activities such as antibacterial and anti-tumor.
Preparation Method:
9-(1H-benzotriazol-1-ylmethyl)-9H-carbazole has many synthetic methods. The following is one of the common synthetic routes:
First, methacrylic acid is reacted with benzotriazole by a nucleophilic addition reaction to obtain 1-methylacrylic acid benzotriazole. Subsequently, the intermediate is subjected to amiodination and hydrogenation to give 9-(1H-benzotriazol-1-ylmethyl)-9H-carbazole.
Safety Information:
Note the following when using and handling 9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole:
-Avoid inhaling dust or contact with skin and eyes, and wear appropriate protective equipment such as gloves, glasses and protective clothing.
-Avoid contact with strong oxidants and strong acids to avoid dangerous reactions.
-When storing and handling, follow proper laboratory procedures to ensure proper ventilation and safety.
Please note that the information provided above is for reference only. The specific operation and use should follow the laboratory and regulations. For specific situations, please consult a professional for detailed guidance.
Nature:
-Appearance: 9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole is a white crystalline solid.
-Melting point: Its melting point range is 235-240 degrees Celsius.
-Solubility: 9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole is soluble in some organic solvents.
Use:
9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole has a variety of uses in chemical research and industrial production, including:
-As an intermediate in organic synthesis, it can be used to synthesize other organic compounds.
-In the field of medicine, it can be used as a raw material for certain drugs and has biological activities such as antibacterial and anti-tumor.
Preparation Method:
9-(1H-benzotriazol-1-ylmethyl)-9H-carbazole has many synthetic methods. The following is one of the common synthetic routes:
First, methacrylic acid is reacted with benzotriazole by a nucleophilic addition reaction to obtain 1-methylacrylic acid benzotriazole. Subsequently, the intermediate is subjected to amiodination and hydrogenation to give 9-(1H-benzotriazol-1-ylmethyl)-9H-carbazole.
Safety Information:
Note the following when using and handling 9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole:
-Avoid inhaling dust or contact with skin and eyes, and wear appropriate protective equipment such as gloves, glasses and protective clothing.
-Avoid contact with strong oxidants and strong acids to avoid dangerous reactions.
-When storing and handling, follow proper laboratory procedures to ensure proper ventilation and safety.
Please note that the information provided above is for reference only. The specific operation and use should follow the laboratory and regulations. For specific situations, please consult a professional for detailed guidance.
Last Update：2024-04-09 21:01:54
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View History
124337-34-4
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