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Trityliso selenocyanate, also known as triphenylmethyl selenocyanate, is an organoselenium compound with the chemical formula (C6H5)3CSeCN. It is a colorless crystalline solid that is sensitive to light and moisture. trityliso selenocyanate is synthesized by the reaction of triphenylmethyl chloride with copper(I) cyanide and selenium. Trityliso selenocyanate is used as a reagent in organic synthesis, particularly for the preparation of selenocyanates and other organoselenium compounds. It is also employed in the synthesis of various pharmaceuticals and agrochemicals due to its unique reactivity and selectivity. However, it should be handled with care, as it is toxic and has potential health risks.

4494-21-7

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4494-21-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4494-21-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,9 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4494-21:
(6*4)+(5*4)+(4*9)+(3*4)+(2*2)+(1*1)=97
97 % 10 = 7
So 4494-21-7 is a valid CAS Registry Number.

4494-21-7Relevant academic research and scientific papers

The chemistry of trityl isoselenocyanate revisited: A preparative and structural investigation

Ben Dahman Andaloussi, Mounir,Mohr, Fabian

experimental part, p. 1276 - 1280 (2010/06/13)

The reaction of trityl chloride with KSeCN gives trityl isoselenocyanate which was structurally characterised by X-ray diffraction. Trityl isoselenocyanate reacts with hydrazine to give trityl selenosemicarbazide and with primary amines to give selenourea derivatives. However, with secondary amines mixtures of selenoureas and substitution products are formed. Trityl selenosemicarbazide undergoes a condensation reaction with salicylaldehyde to give the corresponding trityl selenosemicarbazone. In the case of 2-pyridinecarboxaldehyde, the analogous selenosemicarbazone cannot be isolated, instead a small quantity of the diselenide was isolated from the reaction mixture. The compounds prepared here were fully characterised spectroscopically and several also by X-ray diffraction.

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