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15486-24-5

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15486-24-5 Usage

General Description

Eleutheroside C, often referred to as syringin, is a phenolic compound found in certain plant species such as Eleutherococcus senticosus (Siberian ginseng) and Syringa vulgaris (lilac). It is a biologically active compound that has been shown to possess a wide range of pharmacological properties, including antioxidant, anti-inflammatory, neuroprotective, and anti-cancer effects. Eleutheroside C has been studied for its potential ability to improve cognitive function, enhance energy levels, and reduce stress. It has also been investigated for its potential in treating certain chronic diseases and promoting overall health and well-being. The compound is commonly used in traditional medicine and as a natural supplement to support various aspects of health and wellness.

Check Digit Verification of cas no

The CAS Registry Mumber 15486-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,8 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15486-24:
(7*1)+(6*5)+(5*4)+(4*8)+(3*6)+(2*2)+(1*4)=115
115 % 10 = 5
So 15486-24-5 is a valid CAS Registry Number.

15486-24-5SDS

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 Eleutheroside C

1.2 Other means of identification

Product number -
Other names -

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:15486-24-5 SDS

15486-24-5Relevant articles and documents

Novel nor-harmal alkaloid from Adhatoda vasica

Jain,Koul,Dhar,Atal

, p. 1880 - 1882 (1980)

A novel alkaloid and a galactoside isolated from the roots of Adhatoda vasica have been characterized as 9-acetamido-3,4-dihydropyrido-(3,4-b)-indole and O-ethyl-α-D-galactoside respectively by chemical and spectroscopic methods. In addition sitosterol β-D-glucoside, D-galactose and deoxyvasicinone have also been isolated from the roots of this plant.

Bio-based Surfactants

-

, (2022/03/31)

Bio-based surfactants have great opportunity for use in a variety of applications such as laundry detergents, industrial cleaners, adjuvants, and oil and gas. Surfactants in these applications can be nonionic, anionic, cationic, or amphoteric. Utilizing high oleic soybean oil as a platform chemical, a variety of surfactants and properties can be produced. While early work focused solely on surfactant use in laundry cleaning and fracking, recent work has expanded functional groups and application evaluations in hard surface cleaning. The current invention expands on Battelle's high oleic soybean oil (HOSO) surfactant technology. Use of HOSO overcomes the limitations of regular soybean oil and significantly reduces or eliminates undesirable byproducts in most chemistries. However, with use of select reagents, a few candidates were achievable with regular epoxidized soybean oil (ESO). The HOSO surfactant platform offers several key advantages including: a highly water miscible (not typical of C18 surfactants) and water stable surfactant; ability to adjust and vary hydrophilic-lipophilic (HLB) values for stain removal performance; and increased biodegradability without toxic or persistent by-products.

Glycosyl Bunte Salts: A Class of Intermediates for Sugar Chemistry

Meguro, Yasuhiro,Noguchi, Masato,Li, Gefei,Shoda, Shin-Ichiro

supporting information, p. 76 - 79 (2018/01/17)

S-Glycosyl thiosulfates have been discovered as a new class of synthetic intermediates in sugar chemistry, named "glycosyl Bunte salts" after 19th-century German chemist, Hans Bunte. The synthesis was achieved by direct condensation of unprotected sugars and sodium thiosulfate using a formamidine-type dehydrating agent in water-acetonitrile mixed solvent. The application of glycosyl Bunte salts is demonstrated with transformation reactions into other glycosyl compounds such as a 1-thio sugar, a glycosyl disulfide, a 1,6-anhydro sugar, and an O-glycoside.

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