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α-tert-butyl-β-hydroxy-succinic acid diethyl ester is a complex organic compound with the chemical formula C12H20O4. It is a derivative of succinic acid, featuring a tert-butyl group (a methyl group attached to a carbon atom that is already bonded to three other carbon atoms) at the α-position and a hydroxyl group at the β-position. The diethyl ester indicates that the two carboxylic acid groups of the succinic acid have been esterified with ethanol, resulting in two ethyl ester groups. α-tert-butyl-β-hydroxy-succinic acid diethyl ester is known for its potential applications in the synthesis of various pharmaceuticals and specialty chemicals, particularly as an intermediate in the production of certain drugs and agrochemicals. Its stability and reactivity can be influenced by the presence of the bulky tert-butyl group and the hydroxyl functionality, making it a versatile building block in organic synthesis.

77292-40-1

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77292-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77292-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,9 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77292-40:
(7*7)+(6*7)+(5*2)+(4*9)+(3*2)+(2*4)+(1*0)=151
151 % 10 = 1
So 77292-40-1 is a valid CAS Registry Number.

77292-40-1Downstream Products

77292-40-1Relevant academic research and scientific papers

The Reactions of Lignin with Alkaline Hydrogen Peroxide. Part IV. Products from the Oxidation of Quinone Model Compounds

Gellerstedt, Goeran,Hardell, Hanne-Lise,Lindfors, Eva-Lisa

, p. 669 - 674 (2007/10/02)

Simple para- and orhto-quinoid structures related to lignin have been oxidized with hydrogen peroxide under mild alkaline conditions.Most of the reaction products, i.e. carboxylic acids formed by oxidative cleavage of the quinoid ring together with acids formed by more extensive degradation of the starting materials, were identified after conversion into esters.In addition, small amounts of hydroxylated quinones were found.Mechanisms for the formation of these products are suggested and the significance of the results for the bleaching of mechanical pulps with hydrogen peroxide is briefly discussed.

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