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779339-32-1

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779339-32-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 779339-32-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,9,3,3 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 779339-32:
(8*7)+(7*7)+(6*9)+(5*3)+(4*3)+(3*9)+(2*3)+(1*2)=221
221 % 10 = 1
So 779339-32-1 is a valid CAS Registry Number.

779339-32-1Upstream product

779339-32-1Downstream Products

779339-32-1Relevant articles and documents

Ferrocenecarboselenoic acid: Synthesis and some reactions

Takahashi, Toshinori,Niyomura, Osamu,Kato, Shinzi,Ebihara, Masahiro

, p. 108 - 114 (2013/03/28)

The first ferrocenecarboselenoic acid was synthesized and characterized. The existence of tautomeric equilibrium between the selenol (FcCOSeH) and selenoxo forms (FcCSeOH) in polar solvents was proven by 1H-, 13C- and 77Se-NMR spectra. The selenoxo form exists predominantly in a polar solvent at low temperature below -70 °C. Treatment of this acid with lithium, sodium, and potassium hydrides and with rubidium and cesium fluorides gave the corresponding alkali metal ferrocenecarboselenoates in quantitative yields. Treatment with 4-methylphenyl isocyanate at room temperature led to ferrocenoyl 4-methylphenylcarbamoyl selenide FcCOSeC(O)NHC6H4Me-4 in high yield. A similar reaction with phenyl isothiocyanate formed a mixture of FcCOSeC(S)NHPh and FcCOSeC(SH)=NPh in moderate to good yield. The carboselenoic acid readily reacted with piperidine to give piperidinium ferrocenecarboselenoate in good yield. Air oxidation of this selenoic acid afforded diferrocenoyl selenide as a major product along with diferrocenoyl diselenide. The structures of the selenide (FcCO)2Se and diselenide (FcCOSe)2 were examined by single-crystal X-ray analysis. Copyright

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