4165-32-6 Usage
Uses
Used in Pharmaceutical Industry:
4-Thiazolidinecarboxylicacid,2-methyl-(6CI,7CI,8CI,9CI) is used as a Cysteine prodrug for its protective effects against the fungal T-2 toxin. It serves as a precursor to pharmaceuticals used in the treatment of cataracts, providing a crucial role in the development of therapeutic agents for eye-related conditions.
As a Cysteine Prodrug:
4-Thiazolidinecarboxylicacid,2-methyl-(6CI,7CI,8CI,9CI) is used as a Cysteine prodrug, which means it is a biologically inactive compound that can be metabolized in the body to produce the active form of Cysteine. This property makes it a valuable component in the development of drugs that require Cysteine as an active ingredient.
For Protection Against Fungal T-2 Toxin:
4-Thiazolidinecarboxylicacid,2-methyl-(6CI,7CI,8CI,9CI) serves as a protective agent against the harmful effects of the fungal T-2 toxin, which can cause severe health issues in humans and animals. By incorporating 4-Thiazolidinecarboxylicacid,2-methyl-(6CI,7CI,8CI,9CI) into pharmaceutical formulations, it can help mitigate the negative impacts of T-2 toxin exposure.
In the Treatment of Cataracts:
4-Thiazolidinecarboxylicacid,2-methyl-(6CI,7CI,8CI,9CI) is also used as a precursor to pharmaceuticals that are employed in the treatment of cataracts. Cataracts are a common eye condition that leads to the clouding of the lens in the eye, impairing vision. 4-Thiazolidinecarboxylicacid,2-methyl-(6CI,7CI,8CI,9CI)'s role in the synthesis of such pharmaceuticals contributes to the development of effective treatments for this condition.
Check Digit Verification of cas no
The CAS Registry Mumber 4165-32-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,6 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4165-32:
(6*4)+(5*1)+(4*6)+(3*5)+(2*3)+(1*2)=76
76 % 10 = 6
So 4165-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO2S/c1-3-6-4(2-9-3)5(7)8/h3-4,6H,2H2,1H3,(H,7,8)
4165-32-6Relevant academic research and scientific papers
Azafulvenium methides: New extended dipolar systems
Sutcliffe, Oliver B.,Storr, Richard C.,Gilchrist, Thomas L.,Rafferty, Paul,Crew, Andrew P. A.
, p. 675 - 676 (2007/10/03)
The transient 8π 1,7-dipolar azafulvenium methides 5 and 8 undergo sigmatropic [1,8] H shifts and the acyl derivatives 12 electrocyclise to give novel pyrrolooxazines 13; the related diazafulvenium methide 15 can be intercepted in 8π + 2π cycloadditions with silylated acetylenes.
