116650-34-1
(S)-3-Amino-1,2,3,4-tetrahydrocarbazole
CAS: 116650-34-1
Molecular Formula: C12H14N2
116650-34-1 - Names and Identifiers
| Name | (S)-3-Amino-1,2,3,4-tetrahydrocarbazole |
| Synonyms | (S)-3-amino-1,2,3,4-terahydrocarbazole (3S)-3-aMino-1,2,3,4-terahydrocarbazole (S)-3-Amino-1,2,3,4-tetrahydrocarbazole (3S)-3-AaMino-1,2,3,4-terahydrocarbazole (3S)-3-Amino-1,2,3,4-tetrahydrocarbazole (S)-2,3,4,9-tetrahydro-1H-carbazol-3-amine (3S)-2,3,4,9-tetrahydro-1H-carbazol-3-amine 1H-Carbazol-3-amine, 2,3,4,9-tetrahydro-, (3S)- |
| CAS | 116650-34-1 |
| InChI | InChI=1/C12H14N2/c13-8-5-6-12-10(7-8)9-3-1-2-4-11(9)14-12/h1-4,8,14H,5-7,13H2/t8-/m0/s1 |
116650-34-1 - Physico-chemical Properties
| Molecular Formula | C12H14N2 |
| Molar Mass | 186.25 |
| Density | 1.191±0.06 g/cm3(Predicted) |
| Boling Point | 362.5±42.0 °C(Predicted) |
| pKa | 17.54±0.40(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
| Refractive Index | 1.677 |
| Physical and Chemical Properties | White or pale yellow crystalline powder |
| Use | Rhinitis medication the isomer impurities of rametroban |
116650-34-1 - Introduction
(3S)-3-Amino -1,2,3, 4-tetrahydrocarbazole, also known as L-histidine, is a nitrogen-containing amino acid.
Properties:(3S)-3-amino -1,2,3, 4-tetrahydrocarbazole is a colorless crystalline solid with a characteristic amino acid odor. It is slightly soluble in water and more soluble in acidic conditions. It is an optically active substance and has optical activity.
Purpose:(3S)-3-amino -1,2,3, 4-tetrahydrocarbazole plays an important role in biology. It is one of the basic components of proteins and participates in many biochemical reactions. It is used as a flavor enhancer and nutritional additive in the food industry. In addition, it is also used in the synthesis of biologically active compounds, antioxidants and the preparation of pharmaceuticals.
preparation method:(3S)-3-amino -1,2,3, 4-tetrahydrocarbazole can be synthesized by various methods, and the commonly used method is the synthesis of carbazole. First, benzimidazolone is hydrolyzed to produce imidazolone, and then reacted with p-toluenesulfonamide to obtain the target product.
Safety information:(3S)-3-amino -1,2,3, 4-tetrahydrocarbazole is considered to be a relatively safe compound, but it is still necessary to pay attention to safe operation. Avoid inhalation, contact with skin and eyes. Use appropriate protective measures such as gloves and safety glasses during operation. Follow proper storage methods and avoid contact with strong oxidizing agents. In the event of an accident, contact a doctor immediately and provide a safety data sheet for the chemical.
Properties:(3S)-3-amino -1,2,3, 4-tetrahydrocarbazole is a colorless crystalline solid with a characteristic amino acid odor. It is slightly soluble in water and more soluble in acidic conditions. It is an optically active substance and has optical activity.
Purpose:(3S)-3-amino -1,2,3, 4-tetrahydrocarbazole plays an important role in biology. It is one of the basic components of proteins and participates in many biochemical reactions. It is used as a flavor enhancer and nutritional additive in the food industry. In addition, it is also used in the synthesis of biologically active compounds, antioxidants and the preparation of pharmaceuticals.
preparation method:(3S)-3-amino -1,2,3, 4-tetrahydrocarbazole can be synthesized by various methods, and the commonly used method is the synthesis of carbazole. First, benzimidazolone is hydrolyzed to produce imidazolone, and then reacted with p-toluenesulfonamide to obtain the target product.
Safety information:(3S)-3-amino -1,2,3, 4-tetrahydrocarbazole is considered to be a relatively safe compound, but it is still necessary to pay attention to safe operation. Avoid inhalation, contact with skin and eyes. Use appropriate protective measures such as gloves and safety glasses during operation. Follow proper storage methods and avoid contact with strong oxidizing agents. In the event of an accident, contact a doctor immediately and provide a safety data sheet for the chemical.
Last Update：2024-04-09 21:01:54
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