764-99-8 Usage
Description
Diethylene glycol divinyl ether is a versatile organic compound characterized by its monomeric nature and reactivity, making it a valuable intermediate in various chemical processes and applications.
Uses
Used in Organic Synthesis:
Diethylene glycol divinyl ether is used as a chemical intermediate for its ability to undergo various reactions, such as the addition of isocyanic acid to produce secondary diisocyanates, and hydrolysis to yield glycol and acetaldehyde.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, diethylene glycol divinyl ether is utilized as a key component in the synthesis of various drugs, taking advantage of its reactive properties to form desired molecular structures.
Used in Agrochemicals:
Diethylene glycol divinyl ether is employed in the agrochemical industry as a vital raw material for the development of effective and targeted chemical products, such as pesticides and fertilizers.
Used in Dye Industry:
Diethylene glycol divinyl ether is also used in the dyestuff industry, where its chemical properties contribute to the creation of a wide range of colors and dyes for various applications.
Used in Crosslinking Agents:
Diethylene glycol divinyl ether serves as a crosslinking agent, enhancing the properties of materials by forming covalent bonds between polymer chains, which improves their strength, durability, and stability.
Used in Polymerization:
The polymerization of divinyl ether of diethylene glycol with acidic catalysts results in the formation of crosslinked gels, which have numerous applications in various industries due to their unique properties.
Used in Unsaturated Polyesters:
Diethylene glycol divinyl ether is used in the production of unsaturated polyesters, which are made noncorrosive to metals by reducing hydroxyl and acid numbers through the use of divinyl ethers. This enhancement expands the range of applications for these materials in different industries.
Flammability and Explosibility
Nonflammable
Check Digit Verification of cas no
The CAS Registry Mumber 764-99-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 764-99:
(5*7)+(4*6)+(3*4)+(2*9)+(1*9)=98
98 % 10 = 8
So 764-99-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H10O3.C4H6O/c5-1-3-7-4-2-6;1-3-5-4-2/h5-6H,1-4H2;3-4H,1-2H2
764-99-8Relevant articles and documents
PROCESS FOR PREPARING DIVINYL ETHERS
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Page/Page column 3, (2012/09/05)
Process for preparing divinyl ethers by reacting compounds having two hydroxyl groups (hereinafter referred to as diols) with acetylene, wherein the hydroxyl groups are incompletely reacted with acetylene and the resulting product mixture therefore comprises the monovinyl ether in addition to the divinyl ether andthe monovinyl ether is separated off from the product mixture by extractive distillation in the presence of an extractant.
Purification of alkenyl compounds
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Page column 8, (2008/06/13)
A process for purifying alkenyl compounds having a divalent or trivalent heteroatom in the à-position relative to the double bond by distillation comprises carrying out at least two distillations in which the purified alkenyl compounds are obtained from the gas phase by condensation, where the time between the first distillation after the synthesis of the alkenyl compounds and at least one further distillation is at least one day and the purified alkenyl compounds have an APHA color number of 30.
Liquid-phase fluorination
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, (2008/06/13)
This invention pertains to a method for liquid phase fluorination for perfluorination of a wide variety of hydrogen-containing compounds.