62247-32-9 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
3-(3-Azetidinyl)pyridine is utilized as a building block in organic synthesis for the preparation of various pharmaceutical and agrochemical products. Its unique structure allows for the creation of diverse organic compounds, making it a valuable component in the development of new drugs and agrochemicals.
Used in Chemical Research and Development:
3-(3-Azetidinyl)pyridine is employed as a key intermediate in chemical research and development due to its potential to contribute to the synthesis of a wide range of organic compounds. Its unique properties and structural versatility make it an important target for exploring new chemical reactions and applications.
Used in Biological Activity Studies:
3-(3-Azetidinyl)pyridine is used as a subject of study for its potential biological activities, including anti-inflammatory and antifungal properties. These studies aim to understand and harness its therapeutic potential for various medical and health-related applications.
Check Digit Verification of cas no
The CAS Registry Mumber 62247-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,4 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62247-32:
(7*6)+(6*2)+(5*2)+(4*4)+(3*7)+(2*3)+(1*2)=109
109 % 10 = 9
So 62247-32-9 is a valid CAS Registry Number.
62247-32-9Relevant academic research and scientific papers
HETEROCYCLIC COMPOUNDS FOR MODULATING NR2F6
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, (2021/09/04)
The present disclosure relates to compounds capable of modulating the activity of NR2F6. The compounds of the disclosure may be used in methods for the prevention and/or the treatment of diseases and disorders associated with modulating NR2F6 activity.
Azetidine compounds and process for production
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, (2008/06/13)
Novel azetidine, and particularly 3-pyridyl-azetidine, compounds are disclosed. These compounds are produced from γ-amino alcohols by a sequence comprising disulfonation to produce the sulfonamido-alkylsulfonate and then cyclization to the N-sulfonylazetidine. These azetidine compounds may then be transformed, as desired, to various N-derivatives by substitution of hydrogen or other univalent organic groups on the secondary amine of the azetidine ring.
