3463-92-1 Usage
Uses
Used in Pharmaceutical Industry:
Carpaine is used as a cardiovascular agent for its ability to exhibit positive effects on the heart and circulatory system. Its presence in papaya leaves suggests that it may have potential applications in the development of new drugs or therapies for heart-related conditions.
Used in Nutraceutical Industry:
Carpaine, being a natural compound found in papaya leaves, can also be utilized as an ingredient in the development of nutraceutical products. These products may aim to promote heart health and overall well-being by incorporating the beneficial properties of carpaine.
Used in Research and Development:
Due to its cardiovascular effects, carpaine can be used as a subject of research in the field of pharmacology and medicine. Scientists and researchers can study its mechanisms of action, potential side effects, and ways to enhance its efficacy as a therapeutic agent.
Check Digit Verification of cas no
The CAS Registry Mumber 3463-92-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3463-92:
(6*3)+(5*4)+(4*6)+(3*3)+(2*9)+(1*2)=91
91 % 10 = 1
So 3463-92-1 is a valid CAS Registry Number.
InChI:InChI=1/C28H50N2O4/c1-21-25-19-17-23(29-21)13-9-5-3-8-12-16-28(32)34-26-20-18-24(30-22(26)2)14-10-6-4-7-11-15-27(31)33-25/h21-26,29-30H,3-20H2,1-2H3/t21-,22-,23+,24+,25-,26-/m0/s1
3463-92-1Relevant articles and documents
Enantioselective Total Synthesis of (+)-Azimine and (+)-Carpaine
Sato, Taro,Aoyagi, Sakae,Kibayashi, Chihiro
, p. 3839 - 3842 (2007/10/03)
(Matrix presented) The enantioselective total syntheses of (+)-azimine and (+)-carpaine have been developed, starting with (S)-1,2,4-butanetriol as a single source of chirality. The key common feature in these syntheses involves stereoselective intramolecular hetero-Diels-Alder reaction of an acylnitroso compound. The critical macrocyclic dilactonization of the N-Cbz derivatives of azimic acid and carpamic acid was efficiently achieved by using the Yamguchi macrocyclization conditions.
