ENT-3Β-TIGLOYLOXYKAUR-16-EN-19-O

ENT-3Β-TIGLOYLOXYKAUR-16-EN-19-O - Names and Identifiers

Name	ent-3β-Tigloyloxykaur-16-en-19-oic acid
Synonyms	ENT-3Β-TIGLOYLOXYKAUR-16-EN-19-O ent-3β-Tigloyloxykaur-16-en-19-oic acid 3alpha-Tigloyloxy-ent-kaur-16-en-oic acid ent-3beta-Tigloyloxykaur-16-en-19-oic acid Kaur-16-en-18-oic acid, 3-[[(2E)-2-methyl-1-oxo-2-buten-1-yl]oxy]-, (3α,4α)-
CAS	79406-09-0

ENT-3Β-TIGLOYLOXYKAUR-16-EN-19-O - Physico-chemical Properties

Molecular Formula	C25H36O4
Molar Mass	400.56
Melting Point	153-155℃
Specific Rotation(α)	?74 (c, 0.2 in CHCl3)
Storage Condition	2-8℃

ENT-3Β-TIGLOYLOXYKAUR-16-EN-19-O - Introduction

acid (acid) is a natural product and belongs to the diterpenoid class. Its molecular formula is C26H36O4 and its molecular weight is 412.56g/mol.

This compound is mainly found in some plants, such as Eucommia ulmoides (Eucommia ulmoides) and cedar (Cedrus). It has a white to light yellow crystalline solid form.

UV has a variety of biological activities, such as anti-inflammatory, antioxidant, anti-tumor and antibacterial activities. It has potential application value in the field of pharmacy, especially in the research of anticancer drugs. In addition, it can also be used as a synthetic intermediate for natural products.

The method of preparing the polymer acid is mainly achieved by natural product extraction and chemical synthesis. In the synthesis method, a series of organic synthesis reactions are usually used, such as enolization, alcohol esterification and ester hydrolysis.

Regarding safety information, due to the relatively new nature and application of acid, current safety-related research is still relatively limited. Follow laboratory safety procedures when using, and take care to avoid entering the eyes, skin or inhalation. Wear appropriate personal protective equipment if necessary. At the same time, it is also recommended to carry out detailed safety evaluation and laboratory operation guidance according to specific research needs.

Last Update：2024-04-09 21:04:16