74133-16-7 Usage
Uses
Used in Pharmaceutical Industry:
(2S)-9-hydroxy-2-phenyl-1,5,9-triazacyclotridecan-4-one is used as a potential pharmaceutical compound for its unique structure and possible biological activity. Its complex molecular configuration may contribute to the development of new drugs with novel therapeutic properties.
Used in Medicinal Chemistry Research:
(2S)-9-hydroxy-2-phenyl-1,5,9-triazacyclotridecan-4-one serves as a valuable building block for designing new drugs in the field of medicinal chemistry. Its incorporation into drug candidates can lead to the discovery of innovative therapeutic agents with improved efficacy and selectivity.
Used in Drug Development:
(2S)-9-hydroxy-2-phenyl-1,5,9-triazacyclotridecan-4-one is utilized in drug development processes to explore its potential as a lead compound for creating new medications. Its unique features and synthetic nature make it an attractive candidate for further research and optimization to enhance its medicinal properties.
Check Digit Verification of cas no
The CAS Registry Mumber 74133-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,3 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74133-16:
(7*7)+(6*4)+(5*1)+(4*3)+(3*3)+(2*1)+(1*6)=107
107 % 10 = 7
So 74133-16-7 is a valid CAS Registry Number.
74133-16-7Relevant academic research and scientific papers
95. Asymmetric synthesis of the alkaloids mayfoline and N(1)-Acetyl-N(1)-deoxymayfoline
Kuehne, Paul,Linden, Anthony,Hesse, Manfred
, p. 1085 - 1094 (2007/10/03)
The total syntheses of the spermidine alkaloids (-)-mayfoline (11) and (+)-N(1)-acetyl-N(1)-deoxymayfoline (12) are described. These macrocyclic lactams belong to the most interesting conjugates of the polyamine derivatives very commonly found in nature. The enantioselective syntheses were achieved through resolution of the methyl 3-amino-3-phenylpropanoate (2) by recrystallization of its (+)-L-tartrate salt. Construction of the 13-membered ring ensued through condensation, reductive ring expansion (internal bond cleavage), and finally a transamidation reaction involving a second ring expansion.
