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Ethyl 2,2-diethylglycolate, also known as 2,2-diethyl-1,3-propanediol diethyl ether or 2,2-diethyl-1,3-propanediol diethyl acetal, is an organic compound with the chemical formula C9H20O3. It is a colorless liquid with a mild odor and is soluble in most organic solvents. This chemical is primarily used as a solvent and a chemical intermediate in the synthesis of various compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Ethyl 2,2-diethylglycolate is also known for its ability to act as a stabilizer and a plasticizer in certain applications. It is important to handle this chemical with care due to its potential health and environmental risks, and it is classified as a hazardous substance.

5582-86-5

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5582-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5582-86-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,8 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5582-86:
(6*5)+(5*5)+(4*8)+(3*2)+(2*8)+(1*6)=115
115 % 10 = 5
So 5582-86-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O3/c1-4-8(10,5-2)7(9)11-6-3/h10H,4-6H2,1-3H3

5582-86-5Relevant academic research and scientific papers

Oxazolones as potent inhibitors of 11β-hydroxysteroid dehydrogenase type 1

Sutin, Lori,Andersson, Soeren,Bergquist, Lars,Castro, Victor M.,Danielsson, Eva,James, Stephen,Henriksson, Martin,Johansson, Lars,Kaiser, Christina,Flyren, Katarina,Williams, Meredith

, p. 4837 - 4840 (2008/02/11)

2,5,5-Trisubstituted oxazolones were identified as potent inhibitors of 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1). The synthesis, structure-activity relationship and metabolic stability of these compounds are presented.

Bifunctional Even-electron Ions III. Fragmentation Behaviour of aliphatic Hydroxonium Ions Containing an Additional Carbomethoxy Group

Zahorszky, U. I.

, p. 63 - 69 (2007/10/02)

The primary and subsequent fragmentaations of the bifunctional oxonium ions R-C+(OH)-(CH2)n-COOCH3 (n = 0-5), a, are dominated by functional group interactions.Loss of CH3OH os the only appreciable primary fragmentation of the higher homologues, but for the lowest homologue (a0) this reaction is missing.Instead, CO loss is observed.The next homologue (a1) shows loss of CH2CO besides loss of CH3OH.The mode of the subsequent fragmentations is dependent on the chain length separating the functional group, and formation of cyclic ions is typical of the fragmentation behaviour of a2 and a3.Evidence for proton transfer from the carbonyl oxygen to the methoxy group of a protonated ester group is presented.

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