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2-Methoxy-5-sulfamoylbenzoesaeure-N-(2-diethylaminoethyl)-amid, also known as compound 1, is a complex organic chemical compound with the molecular formula C14H22N2O5S. It is characterized by the presence of a benzoic acid backbone, with a methoxy group at the 2-position and a sulfamoyl group at the 5-position. The molecule also features a diethylaminoethyl amide group attached to the nitrogen atom. 2-Methoxy-5-sulfamoylbenzoesaeure-N-(2-diethylaminoethyl)-amid is of interest in the field of medicinal chemistry, particularly in the development of potential therapeutic agents, due to its unique structure and functional groups that can interact with biological targets. Its synthesis and biological evaluation are subjects of ongoing research to explore its potential applications in drug discovery.

5607-65-8

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5607-65-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5607-65-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,0 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5607-65:
(6*5)+(5*6)+(4*0)+(3*7)+(2*6)+(1*5)=98
98 % 10 = 8
So 5607-65-8 is a valid CAS Registry Number.

5607-65-8Downstream Products

5607-65-8Relevant academic research and scientific papers

Synthesis and Inhibitory Activity on Carbonic Anhydrase of Some New Sulpiride Analogues Studied by Means of a New Method

Botre, Claudio,Botre, Francesco,Jommi, Giancarlo,Signorini, Roberto

, p. 1814 - 1820 (2007/10/02)

The pharmacological activity of several new sulpiride analogues was studied by means of a new approach, based on a potentiometric technique with a pCO2 sensor, capable of detecting carbonic anhydrase inhibition at equilibrium conditions.This procedure gives results stated as percent of inhibition of enzymatic activity (IP, inhibitory power).To prove the reliability of the proposed approach and to study structure-activity relationships, several new molecules were synthesized and tested in comparison with the two sulpiride enantiomers.A possible inhibition mechanism is discussed in terms of experimental evidence obtained from the interactions between the molecular structures of the new synthesized compounds and carbonic anhydrase.

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