468727-31-3 Usage
Uses
Used in Pharmaceutical Research:
(S)-tert-butyl 4-((1H-indol-3-yl)methyl)-2,2-dimethyloxazolidine-3-carboxylate is used as a key compound in pharmaceutical research for its potential biological activities, including anti-inflammatory, antiviral, and antimicrobial properties. Its unique structure allows for the development of novel drug candidates that can target various medical conditions.
Used in Drug Development:
In the drug development industry, (S)-tert-butyl 4-((1H-indol-3-yl)methyl)-2,2-dimethyloxazolidine-3-carboxylate is utilized as a building block for synthesizing new therapeutic agents. Its complex structure and potential biological activities make it a promising candidate for creating innovative medications to address a wide range of medical needs.
Used in Medical Therapeutics:
(S)-tert-butyl 4-((1H-indol-3-yl)methyl)-2,2-dimethyloxazolidine-3-carboxylate is investigated for its potential as a therapeutic agent for various medical conditions. Its anti-inflammatory, antiviral, and antimicrobial properties suggest that it could be a valuable asset in the treatment of different health issues, with ongoing research efforts focused on determining its precise mechanism of action and therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 468727-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,8,7,2 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 468727-31:
(8*4)+(7*6)+(6*8)+(5*7)+(4*2)+(3*7)+(2*3)+(1*1)=193
193 % 10 = 3
So 468727-31-3 is a valid CAS Registry Number.
468727-31-3Relevant academic research and scientific papers
Yamakawa, Takayuki,Ideue, Eiji,Iwaki, Yuzo,Sato, Ayumu,Tokuyama, Hidetoshi,Shimokawa, Jun,Fukuyama, Tohru
, p. 6547 - 6560 (2011)
Three distinct synthetic routes to the 2-prenyl tryptophan core skeleton of tryprostatins and their total syntheses are described. The strategies include a traditional gramine-mediated coupling reaction, Fuerstner indole synthesis, and our radical-mediated indole synthesis from o-alkenylphenyl isocyanide. The establishment of reliable conditions for the radical-mediated construction of indoles via a low-temperature radical initiator V-70 (2,2′-azobis(4- methoxy-2,4-dimethylvaleronitrile)) led to the highly efficient syntheses of tryprostatins A and B.
Total synthesis of tryprostatins a and b
Yamakawa, Takayuki,Ideue, Eiji,Shimokawa, Jun,Fukuyama, Tohru
supporting information; experimental part, p. 9262 - 9265 (2011/02/25)
A reasonable approach to the radical: The establishment of reliable conditions for the radical-mediated construction of indoles enabled the highly efficient synthesis of tryprostatins A and B. Use of the radical initiator 2,2′-azobis(4-methoxy-2,4-dimethylvaleronitrile) has allowed to carry out the radical cyclization at just 30°C, thereby suppressing the formation of by-products. Copyright
