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C38H42N4O10S is a complex organic molecule composed of 38 carbon atoms, 42 hydrogen atoms, 4 nitrogen atoms, 10 oxygen atoms, and 1 sulfur atom. It is a large heterocyclic molecule with various functional groups, such as amine, alcohol, and ester moieties. Due to its structural complexity and potential reactivity, C38H42N4O10S may have pharmaceutical or biological significance. The specific properties and potential uses of C38H42N4O10S would depend on its exact structure and the chemical reactions it can undergo.

442663-63-0

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442663-63-0 Usage

Uses

Used in Pharmaceutical Industry:
C38H42N4O10S is used as a pharmaceutical candidate for [application reason] due to its structural complexity and potential reactivity. Its functional groups, such as amine, alcohol, and ester moieties, may allow it to interact with biological targets and exhibit therapeutic effects.
Used in Chemical Research:
C38H42N4O10S is used as a subject of chemical research for [application reason], such as studying its reactivity, exploring its potential applications, and understanding its chemical properties. C38H42N4O10S's structural complexity and the presence of various functional groups make it an interesting subject for scientific investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 442663-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,2,6,6 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 442663-63:
(8*4)+(7*4)+(6*2)+(5*6)+(4*6)+(3*3)+(2*6)+(1*3)=150
150 % 10 = 0
So 442663-63-0 is a valid CAS Registry Number.

442663-63-0Upstream product

442663-63-0Relevant 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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