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2-Propenamide, 3-[4-(dimethylamino)phenyl]-N-[5-(1H-indol-3-ylmethyl)-1,3,4-thiadiazol- 2-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

518359-89-2

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518359-89-2 Usage

Molecular Structure

Complex molecular structure with a 2-propenamide base, a 3-[4-(dimethylamino)phenyl] substituent, and an N-[5-(1H-indol-3-ylmethyl)-1,3,4-thiadiazol-2-yl] group

Functional Groups

Contains multiple functional groups including an amide, amino, phenyl, indol, and thiadiazol groups

Properties

Likely possesses diverse chemical properties and potential biological activities

Further Study

Additional research and analysis required to determine specific uses and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 518359-89-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,8,3,5 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 518359-89:
(8*5)+(7*1)+(6*8)+(5*3)+(4*5)+(3*9)+(2*8)+(1*9)=182
182 % 10 = 2
So 518359-89-2 is a valid CAS Registry Number.

518359-89-2Downstream Products

518359-89-2Relevant academic research and scientific papers

Synthesis of some newer indolyl-thiadiazolyl-pyrazolines and indolyl-oxadiazolyl-pyrazolines as potential anti-inflammatory agents

Sharma, Shalabh,Srivastava, Virendra Kishor,Kumar, Ashok

, p. 2647 - 2654 (2007/10/03)

Some new 1-acetyl-5-substitutedaryl-3-[5′-(3″ -indolylmethyl)-2′-amino-1′,3′,4′,-thiadiazol- 2′N-yl]-2-pyrazolines 6a-6e and 1-acetyl-5-substitutedaryl-3-[5′-(3″-indolylmethyl)-2′- amino-1′,3′,4′-oxadiazol-2′N-yl]-2-pyrazolines 6′a-6′e have been synthesized by 5-(3′-indolymethyl)-1,3,4-thiadiazolyl)-2-aminosubstitutedchalkones 5a-5e and 5-(3′-indolylmethyl)-1,3,4-oxadiazolyl-2-aminosubstitutedchalkones 5′a-5′e, respectively. All these compounds of the present series have been screened for their anti-inflammatory activity. Compounds 6c and 6′c are found to be most active compound of this series, which show 47.6% and 49.0% inflammation inhibitory activity at a dose of 50 mg/kg p.o., while standard drug phenylbutazone exhibit 45.6% anti-inflammatory activity at same dose. The structure of these compounds has been illustrated by IR and 1H NMR spectra.

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