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γ-Benzyl-γ-(mesitoylamino)butyrolacton is a complex organic chemical compound with the molecular formula C15H19NO3. It is a derivative of butyrolactone, featuring a benzyl group attached to the γ-carbon and a mesitoylamino group (mesitoic acid amide) at the same position. γ-Benzyl-γ-(mesitoylamino)butyrolacton is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions involving butyrolactone and mesitoic acid, and its properties, such as solubility and stability, can be influenced by the specific conditions under which it is prepared. The compound's structure and potential applications make it a subject of interest in the field of organic chemistry and drug development.

79138-07-1

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79138-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79138-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,3 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79138-07:
(7*7)+(6*9)+(5*1)+(4*3)+(3*8)+(2*0)+(1*7)=151
151 % 10 = 1
So 79138-07-1 is a valid CAS Registry Number.

79138-07-1Relevant academic research and scientific papers

α-Aminosaeuren als nucleophile Acylaequivalente, V. Sterisch gelenkte Michael-Addition von Oxazolin-5-on-Anionen an aktivierte Doppelbindungen; Synthese von 1,4-Dicarbonylverbindungen und γ-Oxonitrilen

Wegmann, Helmut,Steglich, Wolfgang

, p. 2580 - 2594 (2007/10/02)

Oxazolin-5-ones with bulky substituents like mesityl or 1-butylcyclohexyl at C-2 undergo triethylamine catalyzed addition to activated olefins exclusively at C-4.Hydrolysis of the derived 4,4-disubstituted 2-mesityl-2-oxazolin-5-ones 9 leads to N-mesitoyl

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