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17018-07-4

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17018-07-4 Usage

Description

GLYCEROL ALPHA,ALPHA'-DIALLYL ETHER is a chemical compound derived from glycerol, which is a type of polyol. It is characterized by the presence of two allyl groups attached to the alpha positions of the glycerol molecule. GLYCEROL ALPHA,ALPHA'-DIALLYL ETHER has potential applications in various industries due to its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
GLYCEROL ALPHA,ALPHA'-DIALLYL ETHER is used as an oral antihyperlipidemic agent for the preparation of polyalcohols. It serves as a key component in the development of medications aimed at reducing high levels of lipids in the blood, which can contribute to cardiovascular diseases and other health issues.

Check Digit Verification of cas no

The CAS Registry Mumber 17018-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,1 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17018-07:
(7*1)+(6*7)+(5*0)+(4*1)+(3*8)+(2*0)+(1*7)=84
84 % 10 = 4
So 17018-07-4 is a valid CAS Registry Number.

17018-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis(prop-2-enoxy)propan-2-ol

1.2 Other means of identification

Product number -
Other names GLYCEROL ALPHA,ALPHA'-DIALLYL ETHER

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:17018-07-4 SDS

17018-07-4Relevant articles and documents

Synthesis method of diallyl glyceryl ether

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Paragraph 0031; 0032; 0033; 0034; 0035; 0036; 0037-0039, (2017/08/25)

The invention discloses a synthesis method of diallyl glyceryl ether. Strong acid ion exchange resin supported SnCl4 is used as a catalyst, allyl glycidyl ether and excessive allyl alcohol undergo an open-loop reaction, the catalyst is recovered by filtering, the excessive allyl alcohol is recovered by distillation, and a target product, diallyl glyceryl ether, is obtained by reduced pressure distillation. Compared with the traditional process, the synthesis method of diallyl glyceryl ether has the advantages that the process flow is short, the reaction condition is mild, and the operation is simple and convenient; the raw materials are readily available, and the product yield is high; the catalyst has low corrosion and can be recycled, and the process is clean and can be put into industrialization easily.

Synthesis of bi- and tetracatenar highly fluorinated compounds for grafting on silicone materials

Malfait, Stéphane,Gérard, Stéphane,Plantier-Royon, Richard,Mignani, Gérard,Portella, Charles

scheme or table, p. 760 - 766 (2011/10/05)

A series of highly fluorinated compounds bearing two or four perfluoroalkyl (RF) chains, with a flexible or rigid core have been synthesized. Radical additions, nucleophilic addition or condensation reactions were implemented for these synthesi

Magnesium hydrogensulfate: A cheap and efficient catalyst for the conversion of epoxides into β-alkoxy alcohols, vicinal-diols, and thiiranes

Salehi, Peyman,Khodaei, Mohammad Mahdi,Zolfigol, Mohammad Ali,Keyvan, Afsaneh

, p. 3041 - 3048 (2007/10/03)

The nucleophilic ring opening reactions of epoxides by aliphatic alcohols and water are achieved efficiently in the presence of catalytic amounts of magnesium hydrogensulfate, Mg(HSO4)2, with high degree of regioselectivity. The reactions are chemoselective and many of the other functional groups such as ethereal carbon oxygen bonds as well as carbon-carbon double bond remain intact under the reaction conditions. Epoxides also react with thiourea or ammonium thiocyanate in the presence of Mg(HSO 4)2 to afford the corresponding thiiranes in good to excellent yields.

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