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17863-69-3

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17863-69-3 Usage

Chemical class

Diacylglycerol

Structure

A glycerol molecule with two decanoyl (C10) fatty acid chains attached

Role

Precursor to the synthesis of triacylglycerols and phospholipids

Applications

Research and pharmaceutical

Involvement

Lipid metabolism and signaling pathways

Therapeutic potential

Cancer, inflammation, and metabolic disorders

Investigation

Role in cell signaling and as a potential target for drug development

Importance

Crucial role in lipid metabolism and potential implications in various biomedical applications

Check Digit Verification of cas no

The CAS Registry Mumber 17863-69-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,6 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17863-69:
(7*1)+(6*7)+(5*8)+(4*6)+(3*3)+(2*6)+(1*9)=143
143 % 10 = 3
So 17863-69-3 is a valid CAS Registry Number.
InChI:InChI=1/C23H44O5/c1-3-5-7-9-11-13-15-17-20(25)22(27)23(28,19-24)21(26)18-16-14-12-10-8-6-4-2/h22,24,27-28H,3-19H2,1-2H3

17863-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-didecanoylglycerol

1.2 Other means of identification

Product number -
Other names 1,2-Didecanoylglycerol

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:17863-69-3 SDS

17863-69-3Relevant articles and documents

Short Communication. A potential chiral derivatizing agent for 1,2-diglycerides

Sonnet, Philip E.,Oliver, James E.,Waters, Roland M.,King, Gregory,Panicker, Sini

, p. 203 - 208 (1995)

Several chiral naphthylacetic acids have been prepared and evaluated as chiral derivatizing reagents for chiral alcohols.Fluorinated acids provide good general HPLC separations of chiral alcohols, especially 1,2-diglycerides.The separations and the 19F-NMR shift differences of pairs of diastereomers are documented. - Keywords: Chiral alcohols; 1,2-diglycerides; Fluoro-(1-naphthyl)acetic acids; Chiral derivatizing agents

Fosaprepitant derivative, synthesis thereof, and use thereof in long acting preparation

-

, (2017/04/03)

The invention relates to a Fosaprepitant derivative, a synthesis thereof, and a use thereof in a long acting preparation. The invention relates to a compound of formula (I), and a salt, an N-oxide, a quaternary ammonium and a stereoisomer thereof. R to R in the formula (I) are as defined in claims. The invention also relates to an intermediate for preparing the compound of formula (I), and a method for preparing the compound of formula (I). The invention further relates to a use of the compound of formula (I) as a drug especially used for preventing chemotherapy induced acute and late nausea and vomiting.

Method for microwave synthesis of glyceryl caprylate-caprate

-

Paragraph 0029-0032; 0034-0037; 0039-0041; 0043-0046; 0048, (2017/07/20)

The invention provides a preparation method for microwave synthesis of glyceryl caprylate-caprate. Caprylate-caprate and glycerin are reacted in the presence of a compound catalyst, and a glyceryl caprylate-caprate product is prepared by microwave synthesis. According to the method, the molar ratio of caprylate and caprate in the glyceryl caprylate-caprate is regulated, catalysis of the compound catalyst is combined, and a frequency band of 300 to 3,000MHz is adopted for microwave synthesis, so that the high-quality glyceryl caprylate-caprate of which the molar ratio of the caprylate and the caprate is controllable can be efficiently and rapidly prepared. According to the method, a high esterification rate can be achieved, and meanwhile, the energy consumption and the production cost of a reaction process can be remarkably reduced.

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