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Oxirane, 2-propenyl-, also known as allyl glycidyl ether (AGE), is a colorless liquid with a molecular formula of C5H8O. It is an epoxide compound, which means it contains a three-membered cyclic ether group. AGE is primarily used as a reactive diluent in the production of epoxy resins, as it helps to lower the viscosity of the resin and improve its processability. It is also used as a crosslinking agent in various applications, such as coatings, adhesives, and composite materials. Due to its high reactivity, AGE can be hazardous and requires proper handling and storage to prevent health and environmental risks.

6790-38-1

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6790-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6790-38-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,9 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6790-38:
(6*6)+(5*7)+(4*9)+(3*0)+(2*3)+(1*8)=121
121 % 10 = 1
So 6790-38-1 is a valid CAS Registry Number.

6790-38-1Relevant academic research and scientific papers

Synthesis of 1,2-epoxy-4-pentene and 1,2,4,5-diepoxypentane by the hydroperoxide oxidation of 1,4-pentadiene

Nozhnin,Mel'nik,Yegorova,Kryukov

, p. 156 - 160 (2007/10/03)

Methods are proposed for the synthesis of 1,2-epoxy-4-pentene and 1,2,4,5-diepoxypentane on the basis of the hydroperoxide oxidation of 1,4-pentadiene. Physicochemical characteristics of 1,2-epoxy-4-pentene that have not been given in the literature are presented.

Synthesis of 1,2,3,4-diepoxybutane from 1,3-butadiene monoxide

Mel'nik,Nozhnin,Grechina,Kryukov,Yegorova,Danilova

, p. 455 - 459 (2007/10/03)

The possibility of producing 1,2,3,4-diepoxybutane by the epoxidation of 1,3-butadiene monoxide with tert-butylhydroperoxide has been demonstrated. The factors complicating the production and isolation of the target product have been studied. As an alternative to 1,2,3,4-diepoxybutane, the synthesis of 1,2,4,5-diepoxypentane is proposed.

Deamination Reactions, 41. Reactions of Aliphatic Diazonium Ions and Carbocations with Ethers

Kirmse, Wolfgang,Jansen, Ulrich

, p. 2607 - 2625 (2007/10/02)

Aliphatic diazonium ions and carbocations were generated by deacylation of appropriate nitrosoureas (1, 5, 9) in alcohol-ether mixtures or in 2-alkoxyethanols.Ethers were generally inferior to alcohols in capturing cationic intermediates.Formation of trialkyloxonium ions led to alkyl exchange or ring opening.The observed reactivity orders were n-butyl > isobutyl for the diazonium ions, allyl > sec-butyl > tert-butyl for the carbocations, methoxy > ethoxy and oxirane > oxetane > tetrahydrofuran for the ethers, indicating the predominance of steric effects.Neighboring group participation in 4-methoxy-1-butanediazonium ions (58) and 4,5-epoxy-1-pentanediazonium ions (74) was detectable but inefficient ( 20percent of cyclic oxonium ions).

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