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1-(3-Chloro-phenyl)-3-[4-(4-methoxy-phenyl)-5-o-tolylazo-thiazol-2-yl]-thiourea is a complex organic compound with the molecular formula C22H18ClN5O2S2. It is characterized by a thiourea core, which is a sulfur-containing analog of urea. The molecule features a 3-chlorophenyl group attached to the thiourea nitrogen, and a 4-(4-methoxyphenyl)-5-o-tolylazo-thiazol-2-yl group attached to the other nitrogen. The o-tolylazo-thiazol-2-yl group is a heterocyclic ring system that includes a thiazole ring fused to a benzene ring, with an o-tolyl (2-methylphenyl) group attached. 1-(3-Chloro-phenyl)-3-[4-(4-methoxy-phenyl)-5-o-tolylazo-thiazol-2-yl]-thiourea is likely to be used in chemical research or as an intermediate in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structure and potential reactivity.

72461-41-7

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72461-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72461-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,6 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72461-41:
(7*7)+(6*2)+(5*4)+(4*6)+(3*1)+(2*4)+(1*1)=117
117 % 10 = 7
So 72461-41-7 is a valid CAS Registry Number.

72461-41-7Downstream Products

72461-41-7Relevant academic research and scientific papers

Potential Antincoplastic Agents: Part IV - N-Aryl-N'-2-(4-p-anisyl-5-arylazothiazolyl)thiocarbamides

Srivastava, S. P.,Upadhaya, J. S.,Sharma, Mahendra Pal

, p. 631 - 632 (2007/10/02)

A number of N-aryl-N'-2-(4-p-anisyl-5-arylazothiazolyl)thiocarbamides (III) have been synthesised by the condensation of 2-amino-4-p-anisyl-5-arylazothiazoles (II) with different aryl isothiocyanates and tested for antitumor-activity.

Synthesis of N-Aryl-N'-2-(4-p-anisyl-5-arylazothiazolyl)thiocarbamides

Srivastava, P. K.,Upadhyaya, J. S.,Yadav, G. S.

, p. 187 - 188 (2007/10/02)

Different N-aryl-N'-2-(4-p-anisyl-5-arylazothiazolyl)thiocarbamides have been synthesized by the condensation of the corresponding 2-amino-4-p-anisyl-5-arylazothiazoles and appropriate aryl isothiocyanates.The intermediates required in these syntheses wer

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