66408-46-6 Usage
Uses
Used in Pharmaceutical Industry:
(16S,19E)-19,20-Didehydro-2α-[(18E)-18,19-didehydroalstphyllan-18-yl]-2,7α-dihydro-1,16-cyclocorynan-17-oic acid methyl ester is used as a potential pharmaceutical compound for its various biological activities. (16S,19E)-19,20-Didehydro-2α-[(18E)-18,19-didehydroalstphyllan-18-yl]-2,7α-dihydro-1,16-cyclocorynan-17-oic acid methyl ester's complex structure and alkaloid nature suggest that it may have applications in the development of new drugs or therapies, particularly in the treatment of various diseases and conditions.
Used in Chemical Research:
(16S,19E)-19,20-Didehydro-2α-[(18E)-18,19-didehydroalstphyllan-18-yl]-2,7α-dihydro-1,16-cyclocorynan-17-oic acid methyl ester is also used as a subject of study in chemical research, where its unique structure and properties can be further explored and understood. Researchers may investigate its potential interactions with other molecules, its reactivity, and its possible applications in the synthesis of other complex organic compounds.
Used in Natural Product Extraction:
(16S,19E)-19,20-Didehydro-2α-[(18E)-18,19-didehydroalstphyllan-18-yl]-2,7α-dihydro-1,16-cyclocorynan-17-oic acid methyl ester can be used in the field of natural product extraction, where it may be isolated from the bark of Alstonia macrophylla Wall and studied for its potential applications in various industries, such as pharmaceuticals, cosmetics, or agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 66408-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,0 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66408-46:
(7*6)+(6*6)+(5*4)+(4*0)+(3*8)+(2*4)+(1*6)=136
136 % 10 = 6
So 66408-46-6 is a valid CAS Registry Number.
66408-46-6Relevant academic research and scientific papers
Gan, Tong,Cook, James M.
, p. 5037 - 5038 (1996)
The partial synthesis of the antiamoebic bisindole alkaloid (-)- macrocarpamine 1 has been completed by coupling (-)-anhydromacrosalhine- methine 2 with plant-derived (+)-pleiocarpamine 3 in anhydrous 0.2 N HCl in THF in 75% yield.
Enantiospecific total synthesis of (-)-anhydromacrosalhine-methine and partial synthesis of the antiamoebic bisindole alkaloid (-)-macrocarpamine
Gan, Tong,Cook, James M.
, p. 1478 - 1483 (2007/10/03)
An enantiospecific total synthesis of (-)-anhydromacrosalhine-methine (7a) was completed from D-(+)-tryptophan via the asymmetric Pictet-Spengler reaction. In addition, a partial synthesis of (-)-anhydromacrosalhine- methine (7a) was carried out from the
