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2-(diethylamino)ethyl-2,2-dicyclohexylpropanoate is a complex organic compound with the molecular formula C25H43NO2. It is a derivative of 2,2-dicyclohexylpropanoic acid, featuring a 2-(diethylamino)ethyl group attached to the molecule. This chemical is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of certain drugs. Its structure, which includes a cyclohexane ring and an aminoethyl group, contributes to its unique chemical properties and reactivity. The compound is characterized by its ability to form salts and has been studied for its potential therapeutic effects. However, it is important to note that the specific uses, safety, and efficacy of 2-(diethylamino)ethyl-2,2-dicyclohexylpropanoate are subject to ongoing research and must be evaluated within the context of scientific studies and regulatory approvals.

3579-28-0

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3579-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3579-28-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3579-28:
(6*3)+(5*5)+(4*7)+(3*9)+(2*2)+(1*8)=110
110 % 10 = 0
So 3579-28-0 is a valid CAS Registry Number.

3579-28-0Downstream Products

3579-28-0Relevant academic research and scientific papers

Synthesis of 2,2-diphenylpropionate derivatives and their effects on larval growth of the silkworm.

Toyomura,Kim,Yoshida,Shiotsuki,Kuwano

, p. 610 - 612 (2007/10/03)

A variety of 2,2-diphenylpropionate derivatives with an amino substituent were synthesized and their effects on larval growth of the silkworm, Bombyx mori, were examined by dietary administration. Of the compounds tested, 3-(4-ethylpiperazin-1-yl)propyl 2,2-diphenylpropionate (3) caused significant prolongation of the larval period. Studies on the structure-activity relationship indicate that a piperazine ring and the bond distances between the nitrogen atom and the ester group were important for this activity. Treatment of compound 3 delayed the increase of ecdysteroid titers in the hemolymph by 3 days compared with that of the control, which correlates with the delay in molting.

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