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5-(4-nitrophenyl)thiazole is a chemical compound with the molecular formula C9H6N2O2S. It is a derivative of thiazole, a heterocyclic compound consisting of a five-membered ring with one sulfur atom and one nitrogen atom. The compound features a 4-nitrophenyl group attached to the thiazole ring, which imparts a nitro group (-NO2) at the para position of the phenyl ring. This chemical is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The presence of the nitro group and the thiazole ring in 5-(4-nitrophenyl)thiazole endows it with potential applications in the development of new compounds with specific biological activities.

3950-26-3

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3950-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3950-26-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,5 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3950-26:
(6*3)+(5*9)+(4*5)+(3*0)+(2*2)+(1*6)=93
93 % 10 = 3
So 3950-26-3 is a valid CAS Registry Number.

3950-26-3Downstream Products

3950-26-3Relevant academic research and scientific papers

Programmed synthesis of arylthiazoles through sequential C-H couplings

Tani, Satoshi,Uehara, Takahiro N.,Yamaguchi, Junichiro,Itami, Kenichiro

, p. 123 - 135 (2014/01/06)

A programmed synthesis of privileged arylthiazoles via sequential C-H couplings catalyzed by palladium or nickel catalysts has been accomplished. This versatile protocol can supply all possible arylthiazole substitution patterns (2-aryl, 4-aryl, 5-aryl, 2

Mild palladium-catalyzed regioselective direct arylation of azoles promoted by tetrabutylammonium acetate

Bellina, Fabio,Lessi, Marco,Manzini, Chiara

, p. 5621 - 5630 (2013/09/12)

A mild, general, and convenient palladium-catalyzed direct arylation of the 5-position of azoles with aryl bromides, efficiently promoted by tetrabutylammonium acetate, is described. 1-Methylpyrazole, oxazole, and thiazole reacted at 70°C in N,N-dimethyla

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