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Benzeneacetic acid, 4-methoxy-, 2-(aminothioxomethyl)hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61904-65-2

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61904-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61904-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,0 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61904-65:
(7*6)+(6*1)+(5*9)+(4*0)+(3*4)+(2*6)+(1*5)=122
122 % 10 = 2
So 61904-65-2 is a valid CAS Registry Number.

61904-65-2Relevant academic research and scientific papers

Design and synthesis of some thiazolotriazolyl esters as anti-inflammatory and analgesic agents

Tozkoparan, Birsen,Aytac, S. Peri,Guersoy, Sule,Aktay, Goeknur

scheme or table, p. 192 - 201 (2012/09/08)

In order to develop potent analgesic/antiinflammatory compounds with reduced ulcerogenic risk, a series of thiazolotriazolyl-carboxylic and acetic acid esters were synthesized and characterized by spectral and elementary analysis. All synthesized compounds were screened for in vivo anti-inflammatory activities in mice by carregeenan-induced paw edema model. The compounds showing 20% reduction in paw edema were also evaluated for their analgesic activities by acetic acid-induced writhing test and the gastric ulceration risk by determining the lipid peroxidation level in stomachs. Among the compounds tested, compounds 1, 4, 6, 7, 8, 1a, 2a, 3a, 4a, 7a, 2b, and 8b showed moderate-to-good anti-inflammatory activity at various doses in any of the measurement intervals. Compounds 7a, 2b, and 8b were the most actives of the series in analgesic activity test. Moreover, compounds 1, 4, and 8 were found to be safe in stomach in respect of free radical production. Springer Science+Business Media, LLC 2010.

2-Amino-5-(substituted or unsubstituted phenylalkyl)-thiadiazoles

-

, (2008/06/13)

2-amino-5-(substituted or unsubstituted phenylalkyl)-thiadiazoles, e.g., 2-amino-5-(4-[phenylbutyl])-thiadiazole, prepared, e.g., by ring closure, of corresponding 1-(substituted or unsubstituted phenylalkanoyl)-thiosemicarbazide in a strong acid medium.

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