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5026-65-3

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5026-65-3 Usage

General Description

Hexadecyl 3,4,5-trihydroxybenzoate, also known as 3,4,5-Trihydroxybenzoic acid hexadecyl ester or simply garcinol, is an organic compound and derivative of benzoic acid. It is a fatty acid ester of a polyphenol compound found in fruits like gooseberries and mangosteen. The compound is also known for its antioxidant, anti-inflammatory, anti-cancer, anti-neurodegenerative, and anti-diabetic properties. The chemical is commonly used in research, especially in fields related to neurodegenerative diseases and cancer. Its anti-inflammatory properties also make it potentially useful in treating conditions like arthritis or inflammatory bowel disease.

Check Digit Verification of cas no

The CAS Registry Mumber 5026-65-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,2 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5026-65:
(6*5)+(5*0)+(4*2)+(3*6)+(2*6)+(1*5)=73
73 % 10 = 3
So 5026-65-3 is a valid CAS Registry Number.
InChI:InChI=1/C23H38O5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-28-23(27)19-17-20(24)22(26)21(25)18-19/h17-18,24-26H,2-16H2,1H3

5026-65-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Hexadecyl Gallate

1.2 Other means of identification

Product number -
Other names Gallic Acid Hexadecyl Ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5026-65-3 SDS

5026-65-3Relevant articles and documents

Design, Synthesis, and Antifungal Activity of Alkyl Gallates Against Plant Pathogenic Fungi In Vitro and In Vivo

Zhao, Xiao-Long,Li, Chun-Qing,Song, Xiao-Mei,Yan, Shuang-Mei,Luo, Du-Qiang

, p. 38 - 43 (2021/02/01)

A series of alkyl gallates was synthesized by reacting gallic acid with the corresponding alcohols. Their structures were determined on the basis of spectroscopic data, including NMR and MS. The antifungal activities of these compounds against plant pathogenic fungi in vitro and in vivo were assessed.

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