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ethyl 1-((3-(4-chlorophenyl)isoxazol-5-yl)methyl)-1H-indole-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

754199-27-4

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754199-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 754199-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,4,1,9 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 754199-27:
(8*7)+(7*5)+(6*4)+(5*1)+(4*9)+(3*9)+(2*2)+(1*7)=194
194 % 10 = 4
So 754199-27-4 is a valid CAS Registry Number.

754199-27-4Downstream Products

754199-27-4Relevant academic research and scientific papers

Design, Synthesis and Characterization of Novel Isoxazole Tagged Indole Hybrid Compounds

Al-Qawasmeh, Raed A.,Al-Nazer, Louy A.,Dawlat-Kari, Sarah A.,Abu-Qatouseh, Luay,Sabri, Salim S.,Aldamen, Murad A.,Sinnokrot, Mutasem

, p. 138 - 148 (2020)

Sixteen new isoxazole tagged indole compounds have been synthesized via copper (I) catalyzed click chemistry of the aryl hydroxamoyl chloride and an indole containing alkyne moiety. The chemical structure of the synthesized compounds has been established using various physicochemical techniques. X-ray single crystal analysis of Ethyl 1-((3-phenylisoxazol-5-yl) methyl)-1H-indole-2-carboxylate (8a) has been analyzed. All compounds were tested for their antibacterial and anticancer activities. The activities for the new compounds were weak against both bacterial strains and the cancer cell lines.

Factor Xa inhibitors based on a 2-carboxyindole scaffold: SAR of neutral P1 substituents

Nazare, Marc,Essrich, Melanie,Will, David W.,Matter, Hans,Ritter, Kurt,Urmann, Matthias,Bauer, Armin,Schreuder, Herman,Dudda, Angela,Czech, Joerg,Lorenz, Martin,Laux, Volker,Wehner, Volkmar

, p. 4191 - 4195 (2007/10/03)

A series of novel, highly potent 2-carboxyindole-based factor Xa inhibitors is described. Structural requirements for neutral ligands, which bind in the S1 pocket of factor Xa were investigated with the 2-carboxyindole scaffold. This privileged fragment assembly approach yielded a set of equipotent, selective inhibitors with structurally diverse neutral P1 substituents.

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