Indole-3-carboxylic acid β-D-glucopyranosyl ester - Names and Identifiers
Indole-3-carboxylic acid β-D-glucopyranosyl ester - Physico-chemical Properties
Molecular Formula | C15H17NO7
|
Molar Mass | 323.3 |
Density | 1.60±0.1 g/cm3(Predicted) |
Boling Point | 626.1±55.0 °C(Predicted) |
Appearance | Powder |
pKa | 12.51±0.70(Predicted) |
Storage Condition | 2-8℃ |
Indole-3-carboxylic acid β-D-glucopyranosyl ester - Introduction
Indole-3-carboxylic acid β-D-glucopyranosyl ester (indole -3-carboxylic acid β-D-glucopyranoside) is a natural plant secondary metabolite, also known as indolyl-3-carboxylic acid glucosides. Its chemical formula is C16H19NO9. The following is a description of some of the properties, uses, preparation methods and safety information of the compound:
Nature:
-Appearance: White or yellowish solid
-Melting Point: about 160-163 ° C
-Solubility: Slightly soluble in water, alcohol and chloroform
Use:
-Pharmacological research: Indole -3-carboxylic acid β-D-glucopyranoside is widely used in pharmacological research, to study its antioxidant, anti-inflammatory, potential pharmacological activity against breast cancer and other diseases.
Method:
The preparation method of indole -3-carboxylic acid β-D-glucopyranoside usually includes the following steps:
1. Synthesis of indole -3-carboxylic acid: first synthesis of indole -3-carboxylic acid, can be obtained by the reaction of acid chloride and indole compounds.
2. Esterification: Indole -3-carboxylic acid reacts with β-D-glucopyranoside to generate β-D-glucopyranoside.
Safety Information:
Last Update:2024-04-10 22:29:15