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3-(4-chloro-phenyl)-4-formyl-sydnone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86870-34-0

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86870-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86870-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,7 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86870-34:
(7*8)+(6*6)+(5*8)+(4*7)+(3*0)+(2*3)+(1*4)=170
170 % 10 = 0
So 86870-34-0 is a valid CAS Registry Number.

86870-34-0Relevant academic research and scientific papers

Synthesis of novel imidazo[2,1-b][1,3,4]thiadiazoles appended to sydnone as anticancer agents

Tegginamath, Gireesh,Kamble, Ravindra R.,Taj, Tasneem,Kattimani, Pramod P.,Meti, Gangadhar Y.

, p. 4367 - 4375 (2013)

A novel series of 3-aryl-4{6′-(6′′-substituted-coumarin- 3′′-yl) imidazo[2,1-b][1,3,4]thiadiazol-2′-yl}-sydnones 5h-5s were synthesized and screened for their anticancer and DNA cleavage activities and analyzed for pharmacological parameters such as toxicity, drug-likeliness, and drug score for oral bioavailability. In vitro toxicity assay was carried out by assessing the survival E. coli AB1157 (wild type) cultures. Some of the compounds have shown significant anticancer activities also.

Design, docking studies and molecular iodine catalyzed synthesis of benzo[a]xanthen-one derivatives as hyaluronidase inhibitors

Kumbar, Mahadev N.,Kamble, Ravindra R.,Kamble, Atulkumar A.,Joshi, Shrinivas D.,Dixit, Sheshagiri R.,Hoskeri, Joy

, p. 2451 - 2460 (2016/10/25)

A series of novel benzo[a]xanthen-11(12H)-one derivatives 4a–m were designed and subjected to docking studies. The title compounds were synthesized from 3-aryl-4-formylsydnones 1a–m, β-naphthol and dimedone in presence of molecular iodine as a catalyst an

Synthesis of novel 2-(3′-aryl-sydnon-4′-ylidene)-5′- substituted-[1,3,4]-thiadiazolylamines and [1,3,4]-thiadiazol-2′-yl-3-oxo- [1,2,4]-triazoles as antimicrobial agents

Bansode, Soujanya,Kamble, Ravindra

body text, p. 867 - 873 (2012/08/14)

The title compounds (3g-n) and (6g-n) were synthesized using 3-arylsydnones as synthons, and the structures were confirmed by IR, 1H NMR, FAB mass and CHN analysis. These compounds were evaluated for their antibacterial and the antifungal activ

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