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51020-86-1

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51020-86-1 Usage

General Description

Licarin A is a natural chemical compound found in the licorice plant, Glycyrrhiza inflata. It is classified as a prenylated isoflavanone and has been found to have various biological activities, including anti-inflammatory, antioxidant, and cytotoxic effects. Licarin A has also been shown to possess potential therapeutic properties for the treatment of inflammatory skin diseases, such as atopic dermatitis and psoriasis. Additionally, research has suggested that licarin A may have potential as an anti-cancer agent, as it has demonstrated the ability to inhibit the growth of certain cancer cells. Studies on licarin A are ongoing, and further research is needed to fully understand its potential uses and mechanism of action.

Check Digit Verification of cas no

The CAS Registry Mumber 51020-86-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,2 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51020-86:
(7*5)+(6*1)+(5*0)+(4*2)+(3*0)+(2*8)+(1*6)=71
71 % 10 = 1
So 51020-86-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H22O4/c1-5-6-13-9-15-12(2)19(24-20(15)18(10-13)23-4)14-7-8-16(21)17(11-14)22-3/h5-12,19,21H,1-4H3/b6-5+/t12-,19-/m1/s1

51020-86-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Licarin A

1.2 Other means of identification

Product number -
Other names dehydrodiisoeugenol

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:51020-86-1 SDS

51020-86-1Relevant articles and documents

Continuous flow study of isoeugenol to vanillin: A bio-based iron oxide catalyst

Filiciotto, Layla,Márquez-Medina, María Dolores,Pineda, Antonio,Balu, Alina M.,Romero, Antonio A.,Angelici, Carlo,de Jong, Ed,van der Waal, Jan C.,Luque, Rafael

, p. 281 - 290 (2019/12/25)

The use of a biorefinery co-product, such as humins, in combination with an iron precursor in a solvent-free method yields a catalytic material with potential use in selective oxidative cleavage reactions. In particular, this catalyst was found active in the hydrogen-peroxide assisted oxidation of a naturally extracted molecule, isoeugenol, to high added-value flavouring agent, vanillin. By carrying out the reaction in continuous flow, not only a better understanding of the reaction mechanism and of the catalyst deactivation can be achieved, but also important insights for optimised conditions can be developed. The findings of this paper could pave the way to a more sustainable process for the production of a valuable food and perfume additive, vanillin.

Task-Specific Catalyst Development for Lignin-First Biorefinery toward Hemicellulose Retention or Feedstock Extension

Qiu, Shi,Guo, Xuan,Huang, Yong,Fang, Yunming,Tan, Tianwei

, p. 944 - 954 (2019/01/08)

A catalytic reductive fractionation method for lignocellulosic biomass, termed lignin-first biorefinery, has emerged, which emphasises preferential depolymerization of the protolignin. However, in most studies, the lignin-first biorefinery is only effective for hardwood that has a high syringyl/guaiacol (S/G) ratio of lignin building blocks, and the degradation of hemicellulose also takes place simultaneously to a certain degree. In this study, two task-specific catalysts were developed to realize hemicellulose retention and feedstock extension through the development of an objective performance–structure relationship. It is found that MoxC/carbon nanotube (CNT) is highly selective in the cleavage of bonds between carbohydrates and lignin and ether bonds in lignin during the catalytic reductive fractionation of hardwood, leading to a carbohydrate (both cellulose and hemicellulose) retention degree in the solid product close to the theoretical maximum and a delignification degree as high as 98.1 %. Ru/CMK-3 is demonstrated to be effective in the catalytic reductive fractionation of softwood and grass, resulting from its weak acidity and high mesoporosity.

Selective Activation of C=C Bond in Sustainable Phenolic Compounds from Lignin via Photooxidation: Experiment and Density Functional Theory Calculations

Zielinski, Morgan,Burke, Luke A.,Samokhvalov, Alexander

, p. 1332 - 1339 (2015/11/10)

Lignocellulosic biomass can be converted to high-value phenolic compounds, such as food additives, antioxidants, fragrances and fine chemicals. We investigated photochemical and heterogeneous photocatalytic oxidation of two isomeric phenolic compounds from lignin, isoeugenol and eugenol, in several nonprotic solvents, for the first time by experiment and the density functional theory (DFT) calculations. Photooxidation was conducted under ambient conditions using air, near-UV light and commercial P25 TiO2 photocatalyst, and the products were determined by TLC, UV-Vis absorption spectroscopy, HPLC-UV and HPLC-MS. Photochemical and photocatalytic oxidation of isoeugenol proceeds via the mild oxidative "dimerization" to produce the lignan dehydrodiisoeugenol (DHDIE), while photooxidation of eugenol does not proceed. The DFT calculations suggest a radical stepwise mechanism for the oxidative "dimerization" of isoeugenol to DHDIE as was calculated for the first time.

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