887000-70-6 Usage
Uses
Used in Medicinal Chemistry:
Propanedinitrile,2-(4-oxo-3-phenyl-2-selenazolidinylidene)is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a promising candidate for the development of new drugs.
Used in Organic Synthesis:
Propanedinitrile,2-(4-oxo-3-phenyl-2-selenazolidinylidene)is used as an intermediate in the synthesis of complex organic molecules. Its selenazolidinylidene moiety can be utilized in various organic reactions to form a wide range of compounds.
Used in Pharmaceutical Research:
Propanedinitrile,2-(4-oxo-3-phenyl-2-selenazolidinylidene)is used as a starting material for the development of new pharmaceutical agents. Its potential biological activities and unique structure make it an interesting target for research in drug discovery.
Used in Chemical Biology:
Propanedinitrile,2-(4-oxo-3-phenyl-2-selenazolidinylidene)is used in chemical biology to study the interactions between small molecules and biological targets. Its unique structure can be used to probe the mechanisms of various biological processes and to develop new tools for biological research.
Check Digit Verification of cas no
The CAS Registry Mumber 887000-70-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,0,0 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 887000-70:
(8*8)+(7*8)+(6*7)+(5*0)+(4*0)+(3*0)+(2*7)+(1*0)=176
176 % 10 = 6
So 887000-70-6 is a valid CAS Registry Number.
887000-70-6Relevant articles and documents
Selenium-containing heterocycles from isoselenocyanates: Synthesis of 2-methylidene-1,3-selenazolidine derivatives
Sommen, Geoffroy L.,Linden, Anthony,Heimgartner, Heinz
, p. 3344 - 3354 (2006)
A convenient and unequivocal synthesis of the title compounds from isoselenocyanates, malononitrile or 2-cyanoacetate, and 1,2-dibromoethane or α-halogenated carboxylic acid derivatives is reported. The proposed reaction mechanism involves in situ cyclization of different halogenated compounds with an intermediate keten-N,Se-acetal, generated by the base promoted nucleophilic addition of the acidic cyanomethylenes to aliphatic and aromatic isoselenocyanates. Chemical and spectroscopic evidence for the structures of the new compounds is presented.
