764-78-3 Usage
Description
ETHYLENE GLYCOL DIVINYL ETHER, 96 is a chemical compound with a 96% purity level, characterized as a colorless, flammable liquid. It is widely recognized for its high reactivity and is utilized as a solvent in various industrial applications, including the production of polymers, resins, and coatings. Additionally, it serves as a chemical intermediate in the synthesis of other compounds. Due to its hazardous nature, it is crucial to handle ETHYLENE GLYCOL DIVINYL ETHER, 96 with care and adhere to safety guidelines.
Uses
Used in Chemical Synthesis Industry:
ETHYLENE GLYCOL DIVINYL ETHER, 96 is used as a chemical intermediate for the synthesis of other compounds, contributing to the development of a diverse range of chemical products.
Used in Polymer Production:
In the polymer industry, ETHYLENE GLYCOL DIVINYL ETHER, 96 is utilized as a solvent, playing a crucial role in the manufacturing process of various polymers.
Used in Resin Manufacturing:
ETHYLENE GLYCOL DIVINYL ETHER, 96 is employed as a solvent in the production of resins, which are essential components in numerous industrial applications.
Used in Coating Industry:
ETHYLENE GLYCOL DIVINYL ETHER, 96 is used as a solvent in the coating industry, aiding in the creation of high-quality coatings for various surfaces.
Given the high reactivity and potential hazards associated with ETHYLENE GLYCOL DIVINYL ETHER, 96, it is imperative that safety precautions are strictly followed during its use in any application.
Check Digit Verification of cas no
The CAS Registry Mumber 764-78-3 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, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 764-78:
(5*7)+(4*6)+(3*4)+(2*7)+(1*8)=93
93 % 10 = 3
So 764-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O2/c1-3-7-5-6-8-4-2/h3-4H,1-2,5-6H2
764-78-3Relevant articles and documents
Direct vinylation of natural alcohols and derivatives with calcium carbide
Teong, Siew Ping,Chua, Ariel Yi Hui,Deng, Shiyun,Li, Xiukai,Zhang, Yugen
supporting information, p. 1659 - 1662 (2017/06/07)
Vinyl ethers are essential synthetic building blocks for organic synthesis, especially for polymer synthesis and highly vinylated polyol substrates. Herein, a transition metal-free, mild, and safe protocol has been developed for direct vinylation of natural alcohols with calcium carbide. Various sugar alcohols, phenol and its derivatives were tested and proved successful using this green methodology. Selectivity of full vinylated products of the reaction decreases with increasing hydroxyl groups because of side reactions occurring under the basic medium. Electron-donating substituted phenols work more efficiently than electron-withdrawing substituted phenols in general. This methodology may provide new insights on selective vinylation of electron-rich biomass-derived materials.
SYNTHESIS OF DIVINYL ETHERS OF DIOLS IN THE KOH-DMSO SYSTEM
Trofimov, B. A.,Kudyakova, R. N.,Oparina, L. A.,Parshina, L. N.,Vins, V. V.
, p. 786 - 790 (2007/10/02)
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