Cloprostenol Impurity 4(5,6-trans-(±)-Cloprostenol)
5,6-trans-(±)-Cloprostenol
CAS: 72029-43-7
Molecular Formula: C22H29ClO6
Cloprostenol Impurity 4(5,6-trans-(±)-Cloprostenol) - Names and Identifiers
Cloprostenol Impurity 4(5,6-trans-(±)-Cloprostenol) - Physico-chemical Properties
| Molecular Formula | C22H29ClO6 |
| Molar Mass | 424.92 |
| Density | 1.321±0.06 g/cm3(Predicted) |
| Boling Point | 628.0±55.0 °C(Predicted) |
| pKa | 4.76±0.10(Predicted) |
Cloprostenol Impurity 4(5,6-trans-(±)-Cloprostenol) - Introduction
5,6-trans-(±)-Cloprostenol is an organic compound with the chemical formula C22H29ClO6. It is a white to off-white crystalline powder with a special isoprene ring structure. The compound is a prostaglandin analog that has the effect of contracting the prostate and causing contractions.
5,6-trans-(±)-Cloprostenol has important applications in the field of veterinary medicine. It is commonly used in reproductive control, mainly for inducing ovulation in animals (especially cattle) and for sperm use. In addition, in veterinary medicine, it is also used to treat endometrial hyperplasia and endometriosis.
The preparation method of 5,6-trans-(±)-Cloprostenol can be obtained by chemical synthesis of prostaglandin E2. The synthetic route includes a multi-step reaction, which needs to go through the steps of esterification, bromination, deprotection, substitution and synthesis.
Regarding safety information, 5,6-trans-(±)-Cloprostenol needs to be used properly and in animal treatment according to doctor's instructions. It may cause skin irritation and eye irritation, so wear gloves and goggles when handling. In addition, care should be taken to avoid inhalation and swallowing during use. If there is accidental contact or misuse, seek medical treatment immediately.
5,6-trans-(±)-Cloprostenol has important applications in the field of veterinary medicine. It is commonly used in reproductive control, mainly for inducing ovulation in animals (especially cattle) and for sperm use. In addition, in veterinary medicine, it is also used to treat endometrial hyperplasia and endometriosis.
The preparation method of 5,6-trans-(±)-Cloprostenol can be obtained by chemical synthesis of prostaglandin E2. The synthetic route includes a multi-step reaction, which needs to go through the steps of esterification, bromination, deprotection, substitution and synthesis.
Regarding safety information, 5,6-trans-(±)-Cloprostenol needs to be used properly and in animal treatment according to doctor's instructions. It may cause skin irritation and eye irritation, so wear gloves and goggles when handling. In addition, care should be taken to avoid inhalation and swallowing during use. If there is accidental contact or misuse, seek medical treatment immediately.
Last Update：2024-04-10 22:29:15
