133453-54-0
27-Norolean-13-en-28-oic acid, 3-[(6-deoxy-β-D-glucopyranosyl)oxy]-, (3β)-
CAS: 133453-54-0
Molecular Formula: C35H56O7
133453-54-0 - Names and Identifiers
| Name | 27-Norolean-13-en-28-oic acid, 3-[(6-deoxy-β-D-glucopyranosyl)oxy]-, (3β)- |
| Synonyms | 27-Norolean-13-en-28-oic acid, 3-[(6-deoxy-β-D-glucopyranosyl)oxy]-, (3β)- |
| CAS | 133453-54-0 |
133453-54-0 - Physico-chemical Properties
| Molecular Formula | C35H56O7 |
| Molar Mass | 588.83 |
| Density | 1.21±0.1 g/cm3(Predicted) |
| Boling Point | 690.4±55.0 °C(Predicted) |
| pKa | 4.72±0.70(Predicted) |
133453-54-0 - Introduction
Propionyl brassinolide is a naturally occurring triterpenoid compound in many plants, with various biological activities. Here is some information about propionyl brassinolide:
Nature:
1. It is a white to almost white crystalline powder, solid at room temperature, with a bitter taste.
2. It can be dissolved in some organic solvents, such as methanol, ethanol, and dimethyl sulfoxide.
Method:
Propionyl brassinolide can be extracted from natural plants or obtained through chemical synthesis. Usually synthesized through multi-step reactions.
Security information:
At present, there is limited research on the toxicity and safety of propionyl brassinolide, and contact with the eyes and skin should be avoided, as well as inhalation. Appropriate protective measures should be taken during use.
Last Update：2024-05-21 11:28:25
133453-54-0 - Introduction
Nature:
Propionyl brassinolide is a naturally occurring triterpenoid compound with 27 carbon atoms, 13 double bonds, and one carboxyl group. It is a white solid that is soluble in organic solvents such as ethanol, chloroform, and dimethyl sulfoxide.
Method:
Propionyl brassinolide is usually extracted from plants, such as certain moss plants. It can also be synthesized through chemical synthesis methods.
Security:
At present, there is no specific toxicity data on propionyl brassinolide, and further research is needed to evaluate its safety. During use, operations should be carried out in accordance with laboratory safety procedures to avoid contact and inhalation, as well as eye and skin contact.
Last Update：2024-05-21 11:29:05
