55623-00-2 Usage
Uses
Used in Pharmaceutical Industry:
(2R)-2,3,4,4aβ,6,7,8,8aβ-Octahydro-4-acetyl-2,5α-methano-5H-pyrido[3,2-b]-1,4-oxazine is used as a pharmaceutical compound for its potential therapeutic applications. (2R)-2,3,4,4aβ,6,7,8,8aβ-Octahydro-4-acetyl-2,5α-methano-5H-pyrido[3,2-b]-1,4-oxazine's unique structure and properties make it a promising candidate for the development of new drugs, particularly in the areas of cancer treatment and other diseases.
Used in Chemical Research:
In the field of chemical research, (2R)-2,3,4,4aβ,6,7,8,8aβ-Octahydro-4-acetyl-2,5α-methano-5H-pyrido[3,2-b]-1,4-oxazine serves as a valuable compound for studying its chemical properties, reactivity, and potential applications in various chemical reactions. Its unique structure allows researchers to explore new synthetic pathways and develop novel chemical methodologies.
Used in Drug Delivery Systems:
Similar to gallotannin, (2R)-2,3,4,4aβ,6,7,8,8aβ-Octahydro-4-acetyl-2,5α-methano-5H-pyrido[3,2-b]-1,4-oxazine can also be employed in the development of drug delivery systems. Its unique structure and properties may enable the design of innovative drug carriers, improving the delivery, bioavailability, and therapeutic outcomes of various pharmaceutical agents.
References
Laing, Warren, White, Tetrahedron Lett., 269 (1975)
Check Digit Verification of cas no
The CAS Registry Mumber 55623-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,2 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55623-00:
(7*5)+(6*5)+(5*6)+(4*2)+(3*3)+(2*0)+(1*0)=112
112 % 10 = 2
So 55623-00-2 is a valid CAS Registry Number.
55623-00-2Relevant academic research and scientific papers
Total synthesis of (-)-Lepistine
Kitabayashi, Yusuke,Yokoshima, Satoshi,Fukuyama, Tohru
supporting information, p. 2862 - 2864 (2014/06/23)
The first total synthesis of (-)-lepistine has been accomplished in 11 steps from (S)-glycidol. The synthesis features construction of the 10-membered ring via an intramolecular epoxide opening by nosylamide, regioselective dehydration to form an enol eth
