132062-77-2 Usage
Uses
Used in Pharmaceutical Synthesis:
POMHEM is used as a building block in the synthesis of pharmaceutical compounds and other organic molecules. Its unique structure allows for the creation of a wide range of molecules with potential therapeutic applications.
Used in Drug Discovery and Development:
Due to its structural elements, POMHEM has the potential to exhibit biological activity, making it a promising candidate for drug discovery and development. Researchers can leverage its properties to design and develop new drugs targeting various diseases and conditions.
Used in Anticancer Applications:
POMHEM has been studied for its potential as an anticancer agent. Its unique structure and the presence of purine, benzyl, and morpholine moieties may contribute to its effectiveness in targeting cancer cells and inhibiting tumor growth.
Used in Scientific Research:
As a versatile chemical compound, POMHEM is utilized in various fields of scientific research, including chemistry, biology, and pharmacology. Researchers can explore its properties and potential applications in creating new molecules and understanding their interactions with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 132062-77-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,6 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132062-77:
(8*1)+(7*3)+(6*2)+(5*0)+(4*6)+(3*2)+(2*7)+(1*7)=92
92 % 10 = 2
So 132062-77-2 is a valid CAS Registry Number.
132062-77-2Relevant academic research and scientific papers
A non-enzymatic, dna template-directed morpholino primer extension approach
Bell, Neil M.,Wong, Raymond,Micklefield, Jason
supporting information; experimental part, p. 2026 - 2030 (2010/07/05)
Extension, please ! A non-enzymatic DNA-template-directed synthesis approach has been developed that allows the morpholino-nucleoside extension of a PNA primer. Equilibration of the ribonucleosides with the template-primer complex, in a noncovalent fashion (see scheme), was shown to be essential for high selectivity. It is envisaged that this chemistry might be used to transcribe nature's genetic material into alternative abiological polymers. (Chemical Equation Representation).
NUCLEOSIDE ANALOGUES WITH A 1,4-DIOXANE, 1,4-OXATHIANE OR 1,4-OXAZINE RING STRUCTURE AS THE CARBOHYDRATE FRAGMENT
Aerschot, Arthur Van,Janssen, Gerard,Herdewijn, Piet
, p. 769 - 777 (2007/10/02)
Pyrimidine and purine nucleoside analogues with a 1,4-dioxane, 1,4-oxathiane or 1,4-oxazine ring structure have been prepared from the corresponding dimesylated seconucleosides by treatment with either sodium hydroxide, sodium sulfide or primary alkylamines.
