3775-17-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
A heterocyclic compound is a cyclic compound containing atoms of at least two different elements, in this case, carbon, nitrogen, oxygen, and sulfur.
Explanation
The compound is often utilized in pharmaceutical research due to its potential biological activity.
Explanation
Studies have been conducted to explore the compound's effectiveness in treating diseases such as cancer and inflammatory conditions.
Explanation
The compound has been studied for its potential antioxidant properties, which could be beneficial in preventing or reducing oxidative stress-related diseases.
Explanation
Research has been conducted to determine the compound's effectiveness against microorganisms, which could have applications in medicine and materials science.
Explanation
1,2,5-Thiadiazolidine, 3,4-diphenyl-, 1,1-dioxide is used as a starting material for the synthesis of other organic compounds with various applications in medicine and materials science.
Heterocyclic compound
Yes
Pharmaceutical research
Commonly used
Potential use
Treatment of various diseases
Antioxidant properties
Investigated
Antimicrobial properties
Investigated
Building block
Synthesis of other organic compounds
Check Digit Verification of cas no
The CAS Registry Mumber 3775-17-5 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 3775-17:
(6*3)+(5*7)+(4*7)+(3*5)+(2*1)+(1*7)=105
105 % 10 = 5
So 3775-17-5 is a valid CAS Registry Number.
3775-17-5Relevant 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.
