60723-27-5 Usage
Uses
Used in Pharmaceutical Industry:
(-)-(S)-Physoperuvine is used as a pharmaceutical compound for its potential therapeutic properties. The expression is: (-)-(S)-Physoperuvine is used as a pharmaceutical compound for its unique structure and potential therapeutic applications.
Used in Research and Development:
(-)-(S)-Physoperuvine is used as a research compound for further investigation into its chemical properties, potential interactions with biopolymers and macromolecules, and possible applications in drug development. The expression is: (-)-(S)-Physoperuvine is used as a research compound for exploring its chemical properties and potential applications in drug development.
Used in Traditional Medicine:
(-)-(S)-Physoperuvine may be used in traditional medicine for its potential medicinal properties derived from the roots of Physalis peruviana Linn. The expression is: (-)-(S)-Physoperuvine is used as a traditional medicine compound for its potential medicinal properties and therapeutic applications.
References
Ray, Sahai, Sethi, Chern. Ind. (London), 454 (1976)
Check Digit Verification of cas no
The CAS Registry Mumber 60723-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,2 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60723-27:
(7*6)+(6*0)+(5*7)+(4*2)+(3*3)+(2*2)+(1*7)=105
105 % 10 = 5
So 60723-27-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO/c1-9-7-3-2-5-8(9,10)6-4-7/h7,10H,2-6H2,1H3
60723-27-5Relevant academic research and scientific papers
A stereoselective synthesis of (+)-physoperuvine using a tandem aza-Claisen rearrangement and ring closing metathesis reaction
Zaed, Ahmed M.,Swift, Michael D.,Sutherland, Andrew
supporting information; experimental part, p. 2678 - 2680 (2009/09/08)
A stereoselective synthesis of (+)-physoperuvine, a tropane alkaloid from Physalis peruviana Linne has been developed using a one-pot tandem aza-Claisen rearrangement and ring closing metathesis reaction to form the key amino-substituted cycloheptene ring
Enantioselective ring opening of tropinone. a new entry into tropane alkaloids
Majewski, Marek,Lazny, Ryszard,Ulaczyk, Agnieszka
, p. 754 - 761 (2007/10/03)
The lithium enolate of tropinone reacts with alkyl chloroformates to give 6-N-carboalkoxy-N-methyl-2-cycloheptenones (4). These compounds can be produced enantioselectively, in up to 95% ee, if chiral lithium amides (derived from optically pure amines 5-7
