2,3-Thioepoxy Madol
Androstan-17-ol, 2,3-epithio-17-methyl-, (2a,3a,5a,17b)-
CAS: 4267-80-5
Molecular Formula: C20H32OS
2,3-Thioepoxy Madol - Names and Identifiers
2,3-Thioepoxy Madol - Physico-chemical Properties
| Molecular Formula | C20H32OS |
| Molar Mass | 320.54 |
| Density | 1.113 |
| Melting Point | 168-169℃ |
| Boling Point | 427.0±38.0 °C(Predicted) |
| pKa | 15.16±0.60(Predicted) |
| Storage Condition | 2-8℃ |
| Use | Intermediate |
2,3-Thioepoxy Madol - Introduction
Androstan-17-ol, 2,3-epithio-17-methyl-, (2a,3a,5a,17b)-(Androstan-17-ol, 2,3-epithio-17-methyl-, (2a,3a,5a,17b)-) is an organic compound with the formula C21H32OS and a molecular weight of 332.54g/mol.
Androstan-17-ol, 2,3-epithio-17-methyl-, (2a,3a,5a,17b)-is a colorless crystal with a strong pungent odor. It is a stable compound that can be stored for a long time at room temperature. It has low solubility and is soluble in ethanol, acetone and dimethyl sulfoxide.
Androstan-17-ol, 2,3-epithio-17-methyl-, (2a,3a,5a,17b)-is commonly used as an intermediate in the pharmaceutical field. It has important applications in the synthesis of steroid hormones and other drugs. In addition, it is also used in research fields, such as biological activity research and catalysts for chemical reactions.
Androstan-17-ol, the preparation method of 2,3-epithio-17-methyl-, (2a,3a,5a,17b)-mainly includes two ways of synthesis and extraction. Synthetic methods involve chemical synthesis and enzyme-catalyzed reactions, with enzyme-catalyzed reactions being one of the more commonly used methods. The extraction method is generally obtained by extraction and purification from biological tissues of animals or plants.
Regarding safety information, Androstan-17-ol, 2,3-epithio-17-methyl-, (2a,3a,5a,17b)-is an organic compound with certain irritation and toxicity. Care should be taken to wear appropriate personal protective equipment such as gloves and glasses during handling. In addition, it should be kept away from fire sources and avoid contact with oxidants. If contact with skin or eyes, rinse immediately with plenty of water and seek medical help. The use and handling of this compound should comply with relevant regulations and safe practices.
Androstan-17-ol, 2,3-epithio-17-methyl-, (2a,3a,5a,17b)-is a colorless crystal with a strong pungent odor. It is a stable compound that can be stored for a long time at room temperature. It has low solubility and is soluble in ethanol, acetone and dimethyl sulfoxide.
Androstan-17-ol, 2,3-epithio-17-methyl-, (2a,3a,5a,17b)-is commonly used as an intermediate in the pharmaceutical field. It has important applications in the synthesis of steroid hormones and other drugs. In addition, it is also used in research fields, such as biological activity research and catalysts for chemical reactions.
Androstan-17-ol, the preparation method of 2,3-epithio-17-methyl-, (2a,3a,5a,17b)-mainly includes two ways of synthesis and extraction. Synthetic methods involve chemical synthesis and enzyme-catalyzed reactions, with enzyme-catalyzed reactions being one of the more commonly used methods. The extraction method is generally obtained by extraction and purification from biological tissues of animals or plants.
Regarding safety information, Androstan-17-ol, 2,3-epithio-17-methyl-, (2a,3a,5a,17b)-is an organic compound with certain irritation and toxicity. Care should be taken to wear appropriate personal protective equipment such as gloves and glasses during handling. In addition, it should be kept away from fire sources and avoid contact with oxidants. If contact with skin or eyes, rinse immediately with plenty of water and seek medical help. The use and handling of this compound should comply with relevant regulations and safe practices.
Last Update：2024-04-09 20:52:54
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