17018-07-4

Basic information

• Product Name: GLYCEROL ALPHA,ALPHA'-DIALLYL ETHER
• Synonyms: glycerol,1,3-diallyldiether;glycerol,1,3-diallylether;1,3-Bis-(allyloxy)-2-hydroxypropane;1,3-Bis(allyloxy)-2-propanol;1-O,3-O-Diallylglycerin;Glycerin 1,3-diallyl ether;Glycerol alpha,alpha-diallyl ester;1,3-Diallyloxy-2-propanol GDAE
• CAS NO: 17018-07-4
• Molecular Formula: C₉H₁₆O₃
• Molecular Weight: 172.22
• Mol File: 17018-07-4.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 106°C 6mm
• Flash Point: 99.6°C
• Appearance: /
• Density: 0,98 g/cm3
• Refractive Index: 1.4530-1.4550
• PKA: 13.83±0.20(Predicted)
• CAS DataBase Reference: GLYCEROL ALPHA,ALPHA'-DIALLYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: GLYCEROL ALPHA,ALPHA'-DIALLYL ETHER(17018-07-4)
• EPA Substance Registry System: GLYCEROL ALPHA,ALPHA'-DIALLYL ETHER(17018-07-4)

Safety Data

• RTECS: UA7380500
• Hazardous Substances Data: 17018-07-4(Hazardous Substances Data)

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.

Upstream product

• 35466-83-2 allyl methyl carbonate 
• 56-81-5 glycerol 
• 106-89-8 epichlorohydrin 
• 106-92-3 Allyl glycidyl ether 
• 107-18-6 allyl alcohol 
• 96-23-1 1,3-Dichloro-2-propanol 

Downstream Products

• 338459-13-5 3,7,11,15,19-penta-O-benzyl-1,5,9,13,17-pentaoxacycloicosane-3,7,11,15,19-pentaol 
• 338459-06-6 6,10,14-tri-O-benzyl-4,8,12,16-tetraoxanonadecane-1,18-diene-6,10,14-triol 
• 338458-76-7 10-O-benzyl-1,2:18,19-di-O-isopropylidene-4,8,12,16-tetraoxanonadecane-1,2,6,10,14,18,19-heptaol 
• 338459-07-7 2,6,10-tri-O-benzyl-4,8-dioxaundecane-1,2,6,10,11-pentaol 
• 338459-05-5 10-O-benzyl-4,8,12,16-tetraoxanonadecane-1,18-diene-6,10,14-triol 
• 196497-40-2 6-O-benzyl-1,2:10,11-diepoxy-4,8-dioxaundecane-6-ol 
• 93625-24-2 6-O-benzyl-4,8-dioxaundecane-1,10-dien-6-ol 
• 75-30-9 2-iodo-propane 

Relevant articles and documents

Synthesis method of diallyl glyceryl ether

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

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

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.