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2,2,4,4-tetradeuterocyclobutane-1-carbonitrile is a deuterated derivative of cyclobutane-1-carbonitrile, a cyclic compound with a carbonitrile functional group. Deuteration refers to the replacement of hydrogen atoms with deuterium (an isotope of hydrogen with one proton and one neutron), which can be useful in various applications, such as in NMR spectroscopy to enhance signal resolution or in chemical reactions to study kinetic isotope effects. In this specific compound, four hydrogen atoms are replaced with deuterium atoms, resulting in a molecular formula of C4D4N. The compound retains the cyclobutane ring structure, with the carbonitrile group (-CN) attached to one of the carbon atoms. This modification can influence the compound's physical and chemical properties, such as reactivity, stability, and solubility, making it a valuable tool in organic chemistry research and development.

30505-19-2

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30505-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30505-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,5,0 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30505-19:
(7*3)+(6*0)+(5*5)+(4*0)+(3*5)+(2*1)+(1*9)=72
72 % 10 = 2
So 30505-19-2 is a valid CAS Registry Number.

30505-19-2Downstream Products

30505-19-2Relevant academic research and scientific papers

Co(II)PORPHYRIN CATALYZED ISOMERIZATION OF BICYCLOBUTANECARBONITRILE

Miki, Sadao,Matsumura, Sei-ichiro,Ohno, Toshinobu,Yoshida, Zen-ichi

, p. 3669 - 3672 (1986)

In the presence of catalytic amount of TPPCo(II), bicyclobutane-1-carbonitrile easily isomerized to cyclobutane-1-carbonitrile in 60-70 percent yield.Reaction behavior of other electronegative substituted bicyclobutanes in the presence of TPPCo(II) was also investigated.

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