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C31H31N3O9S is a complex organic molecule composed of 31 carbon atoms, 31 hydrogen atoms, 3 nitrogen atoms, 9 oxygen atoms, and 1 sulfur atom. Its chemical structure suggests that it is likely a large organic molecule, possibly a peptide or a peptide derivative, due to the presence of nitrogen and oxygen atoms. The inclusion of sulfur also indicates that this molecule may possess biological activity, as sulfur is often found in biologically active compounds such as proteins and enzymes. Further analysis and experimentation are required to determine the exact nature and properties of this molecule.

308359-33-3

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308359-33-3 Usage

Uses

Given the information provided, there are no specific applications mentioned for C31H31N3O9S. However, based on its chemical composition and the presence of sulfur, it can be hypothesized that this molecule may have potential uses in various industries, particularly in the pharmaceutical and biotechnology sectors, due to its potential biological activity. Further research would be needed to explore and confirm its specific applications and benefits in these or other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 308359-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,8,3,5 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 308359-33:
(8*3)+(7*0)+(6*8)+(5*3)+(4*5)+(3*9)+(2*3)+(1*3)=143
143 % 10 = 3
So 308359-33-3 is a valid CAS Registry Number.

308359-33-3Upstream product

308359-33-3Relevant academic research and scientific papers

Total synthesis of ecteinascidin 743

Endo, Atsushi,Yanagisawa, Arata,Abe, Masanao,Tohma, Shigemitsu,Kan, Toshiyuki,Fukuyama, Tohru

, p. 6552 - 6554 (2007/10/03)

The total synthesis of ecteinascidin 743 (1), an extremely potent antitumor agent, has been accomplished. The synthesis features Ugi's 4CC reaction, intramolecular Heck reaction, phenol-aldehyde cyclization, and acid-induced intramolecular sulfide formation. Copyright

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