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Ethyl 1-[(phenylcarbamoyl)amino]cyclohexanecarboxylate is a complex organic compound with the chemical formula C16H22N2O3. It is a derivative of cyclohexane, with a carbamoyl group (-CO-NH2) attached to a phenyl ring, and an amino group (-NH2) connected to the cyclohexane ring. ethyl 1-[(phenylcarbamoyl)amino]cyclohexanecarboxylate is characterized by its ester functionality, as it contains an ethyl group (-CH2CH3) bonded to a carboxylate group (-COO-). It is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound's structure and properties make it a versatile building block in organic chemistry, particularly in the development of drugs and other bioactive molecules.

4896-09-7

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4896-09-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4896-09-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,9 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4896-09:
(6*4)+(5*8)+(4*9)+(3*6)+(2*0)+(1*9)=127
127 % 10 = 7
So 4896-09-7 is a valid CAS Registry Number.

4896-09-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-(phenylcarbamoylamino)cyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

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More Details:4896-09-7 SDS

4896-09-7Relevant academic research and scientific papers

Synthesis, selective aldose reductase inhibitory profile and antihyperglycaemic potential of certain parabanic acid derivatives

Nabil Aboul-Enein,El-Azzounya,Maklad,Attia,Wiese

, p. 329 - 350 (2007/10/03)

Synthesis and aldose reductase inhibitory profile of certain parabanic acid derivatives 1a-p is described. Also, the antihyperglycaemic potential of these compounds was studied. The most active inhibitors in this series were compounds 1 g, 1p, and 1o which showed inhibitory activity, 36.6, 90 and 91% respectively, at concentration 1 × 10-4. Their IC50 were 2 × 10-6, 7.5 × 10-8 and 5 × 10-8, respectively. Compound 1o exhibited pronounced antihyperglycaemic effect.

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