3775-19-7 Usage
Type of compound
Heterocyclic compound
It contains a five-membered ring with a sulfur atom and two nitrogen atoms.
Potential applications
Pharmaceutical intermediate
The compound may be used as a building block or precursor in the synthesis of pharmaceuticals.
Potential applications
Ligand in coordination chemistry
It can be used to form complexes with metal ions, which may have various applications in chemistry and materials science.
Potential applications
Development of new materials
The compound may be used in the creation of new materials with specific properties, such as conductivity or magnetism.
Potential applications
Organic synthesis
It can be used as a reagent or intermediate in the synthesis of other organic compounds.
Specific properties and uses
Depend on application and context
The properties and potential uses of the compound may vary depending on the specific application and the conditions in which it is used.
Check Digit Verification of cas no
The CAS Registry Mumber 3775-19-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3775-19:
(6*3)+(5*7)+(4*7)+(3*5)+(2*1)+(1*9)=107
107 % 10 = 7
So 3775-19-7 is a valid CAS Registry Number.
3775-19-7Relevant academic research and scientific papers
Oxidation of 1,2,5-Thiadiazolidine 1,1-Dioxides: Synthesis of Diaryl 1,2-Diketones
Pansare, Sunil V.,Malusare, Mahesh G.
, p. 671 - 672 (2007/10/03)
Treatment of 3,4-diaryl 1,2,5-thiadiazolidine 1,1-dioxides with selenium dioxide followed by hydrolysis of the crude oxidation product furnishes the corresponding diaryl 1,2-diketones. Symmetrical and unsymmetrical diketones are readily prepared by this method.
Intramolecular imine cross-coupling in dibenzylidine sulfamides: Synthesis of unsymmetrical 1,2-diaryl ethanediamines
Pansare, Sunil V.,Malusare, Mahesh G.
, p. 2859 - 2862 (2007/10/03)
Intramolecular reductive cross-coupling of unsymmetrical dibenzylidene sulfamides generates the corresponding cyclic sulfamides in good yield. These intermediates are readily converted to the free, unsymmetrical 1,2-diaryl ethanediamines.
