24050-16-6 Usage
Description
2-METHYLTHIAZOLIDINE is a low molecular-weight thiol compound that is commonly found in Ehrlich Ascites Tumor Cells (EATC) and mouse liver homogenate. It possesses unique chemical properties that make it a valuable compound for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
2-METHYLTHIAZOLIDINE is used as a source of low molecular-weight thiol compounds for various pharmaceutical applications. Its presence in EATC and mouse liver homogenate makes it a promising candidate for research and development in the field of drug discovery and therapeutics.
Used in Research and Development:
2-METHYLTHIAZOLIDINE is used as a source of low molecular-weight thiol compounds in research and development, particularly in the study of Ehrlich Ascites Tumor Cells and mouse liver homogenate. Its unique properties and presence in these biological systems make it an important compound for understanding various biological processes and developing new therapeutic strategies.
Used in Biochemical Studies:
2-METHYLTHIAZOLIDINE is used as a source of low molecular-weight thiol compounds in biochemical studies, where it can help researchers investigate the role of thiol compounds in various biological processes and their potential applications in medicine and biotechnology.
Check Digit Verification of cas no
The CAS Registry Mumber 24050-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,5 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24050-16:
(7*2)+(6*4)+(5*0)+(4*5)+(3*0)+(2*1)+(1*6)=66
66 % 10 = 6
So 24050-16-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NS/c1-4-5-2-3-6-4/h4-5H,2-3H2,1H3
24050-16-6Relevant articles and documents
Mechanistic Studies on Thiazolidine Formation in Aldehyde/Cysteamine Model Systems
Huang, Tzou-Chi,Huang, Lee-Zen,Ho, Chi-Tang
, p. 224 - 227 (2007/10/03)
A mechanism was proposed to elucidate the formation of a thiazolidine in aldehyde/cysteamine model systems. Buffer dramatically promotes thiazolidine formation from formaldehyde and cysteamine. Phosphate tends to stabilize the primary carbocation formed, and this may lead to completion of the cyclization by attack of the amino nitrogen on the activated carbon. Protic solvent, by removing the water molecule, further enhances thiazolidine formation. Redox reaction catalyzed by phosphate ions results in the conversion of thiazolidine to the corresponding thiazoline through hydride transfer.
