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4-carbomethoxy-2-(4-nitrophenyl)-δ2-thiazoline is a complex organic compound with the molecular formula C11H8N2O4S. It features a thiazoline ring, which is a five-membered heterocyclic ring containing sulfur and nitrogen atoms. The molecule has a 4-nitrophenyl group attached to the thiazoline ring, which contributes to its chemical properties. The carbomethoxy group (ester of carboxylic acid) is present at the 4-position of the thiazoline ring, further influencing its reactivity and stability. 4-carbomethoxy-2-(4-nitrophenyl)-δ2-thiazoline is often used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and potential biological activity.

2519-90-6

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2519-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2519-90-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2519-90:
(6*2)+(5*5)+(4*1)+(3*9)+(2*9)+(1*0)=86
86 % 10 = 6
So 2519-90-6 is a valid CAS Registry Number.

2519-90-6Relevant academic research and scientific papers

The Synthesis and Biological Evaluation of Anithiactin A/Thiasporine C and Analogues

Lamb, Richard A.,Badart, Michael P.,Swaney, Brooke E.,Gai, Sinan,Baird, Sarah K.,Hawkins, Bill C.

, p. 1829 - 1833 (2015/12/26)

The synthesis of anithiactin A has been achieved in four steps. Several closely related analogues were synthesised and their biological activity against colon and breast cancer cell lines evaluated. Anithiactin A was found not to be cytotoxic even at a hi

Copper-catalyzed oxidation of azolines to azoles

Dawsey, Anna C.,Li, Vincent,Hamilton, Kimberly C.,Wang, Jianmei,Williams, Travis J.

experimental part, p. 7994 - 8002 (2012/08/08)

We report herein convenient, aerobic conditions for the oxidation of thiazolines to thiazoles and data regarding the oxidation mechanism. These reactions feature operationally simple and environmentally benign conditions and proceed in good yield to afford the corresponding azoles, thus enabling the inexpensive preparation of valuable molecular building blocks. Incorporation of a novel diimine-ligated copper catalyst, [(MesDABMe) CuII(OH2)3]2+ [-OTf] 2, provides increased reaction efficiency in many cases. In other cases copper-free conditions involving a stoichiometric quantity of base affords superior results.

Titanium(IV)-mediated tandem deprotection-cyclodehydration of protected cysteine N-amides: Biomimetic syntheses of thiazoline- and thiazole-containing heterocycles

Raman, Prakash,Razavi, Hossein,Kelly, Jeffery W.

, p. 3289 - 3292 (2007/10/03)

(matrix presented) The scope and limitations of TiCl4-mediated Δ2-thiazoline synthesis via tandem deprotection-dehydrocyclization of trityl-protected cysteine N-amides is presented. While chemical yields are acceptable (53-96%), the

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