3-beta-O-(trans-p-Coumaroyl)maslinic acid

3-beta-O-(trans-p-Coumaroyl)maslinic acid - Names and Identifiers

Name	3-beta-O-(trans-p-Coumaroyl)maslinic acid
Synonyms	3-O-trans-Cumaroylmaslininsaeure 3β-O-(trans-p-Coumaroyl)maslinic acid 3-beta-O-(trans-p-Coumaroyl)maslinic acid 3beta-O-(trans-p-Coumaroyl)-2alpha-hydroxyolean-12-en-28-oic acid Olean-12-en-28-oic acid, 2-hydroxy-3-[[(2E)-3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-, (2α,3β)-
CAS	35482-91-8

3-beta-O-(trans-p-Coumaroyl)maslinic acid - Physico-chemical Properties

Molecular Formula	C39H54O6
Molar Mass	618.84
Appearance	Powder
Storage Condition	2-8℃

3-beta-O-(trans-p-Coumaroyl)maslinic acid - Introduction

3-beta-O-(trans-p-Coumaroyl)maslinic acid is a natural triterpenic acid compound with various chemical properties and biological activities. Here are details about the compound:

Properties: 3-beta-O-(trans-p-Coumaroyl)maslinic acid is a white to yellow crystalline solid with moderate solubility. It is an acidic compound that dissolves in water, alcohol and Ester solvents. In addition, it is also a photosensitive compound and needs to be protected from light.

Uses: 3-beta-O-(trans-p-Coumaroyl)maslinic acid has a variety of pharmacological and biological activities and has been widely studied. It is considered to have antioxidant, anti-inflammatory, anti-cancer, antibacterial, antiviral and anti-diabetic effects. Due to its pharmacological activity, it can be used in the fields of drug research and development, food additives and health products.

Preparation method: 3-beta-O-(trans-p-Coumaroyl)maslinic acid can be extracted from plants or obtained by synthetic methods. A common source of extraction is oak bark, which is rich in equine acid. Methods of chemical synthesis include the synthesis of target compounds by catalytic hydrogenation, alkylation or aromatization reactions using known synthetic routes and reaction conditions.

Safety Information: Limited toxicity and safety information for 3-beta-O-(trans-p-Coumaroyl)maslinic acid. However, according to relevant research, it is considered safe within a certain concentration range. However, as a potentially biologically active compound, standard chemical laboratory practices and personal protective measures are still required for use. During use, it is recommended to wear gloves, goggles and laboratory coats to avoid skin contact and inhalation. If necessary, it should be operated under well-ventilated conditions. It is best used under professional guidance and in accordance with the laws and regulations of the relevant region.

Last Update：2024-04-09 21:32:49