35995-21-2 Usage
Uses
Used in Pharmaceutical Industry:
3-Hydroxy-1-ethylazetidin-2-one is used as a chiral intermediate for the synthesis of pharmaceutical compounds, specifically those with sedative and anticonvulsant properties. Its unique structure and reactivity make it a valuable component in the development of drugs targeting various neurological conditions.
Used in Heterocyclic Compound Preparation:
In the field of organic chemistry, 3-Hydroxy-1-ethylazetidin-2-one is utilized as a key building block in the preparation of various heterocyclic compounds. Its structural versatility allows for the creation of a wide range of complex molecules with diverse applications in medicine and other industries.
Used in Anti-inflammatory and Analgesic Drug Development:
3-Hydroxy-1-ethylazetidin-2-one is studied for its potential anti-inflammatory and analgesic properties, making it a promising candidate for the development of new drugs aimed at treating pain and inflammation. Its ability to modulate biological pathways involved in these conditions positions it as a valuable asset in the search for more effective therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 35995-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,9 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35995-21:
(7*3)+(6*5)+(5*9)+(4*9)+(3*5)+(2*2)+(1*1)=152
152 % 10 = 2
So 35995-21-2 is a valid CAS Registry Number.
35995-21-2Relevant academic research and scientific papers
Aryloxy and aryloxyalklazetidines as antiarrhythmic and anticonvulsant agents
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, (2008/06/13)
Methods of treating cardiac arrhythmias and convulsions in warm-blooded animas and pharmaceutical compositions therefor are disclosed. The compounds useful in the methods of treatment and compositions are represented by the formula STR1 where n is 0 to 3 and R is H, C1 -C4 alkyl or arylalkyl and Ar is phenyl or substituted phenyl.
Preparation of 3-Azetidinols with Non-Bulky 1-Alkyl Substituents
Higgins, Robert H.,Eaton, Quentin L.,Worth, Leroy,Peterson, Myra V.
, p. 255 - 259 (2007/10/02)
Cyclization of either the tetrahydropyranyl or trimethylsilyl ether of 1-(alkylamino)-3-chloro-2-propanols 1 followed by cleavage of the azetidinyl ether provides a general method for the preparation of 1-alkyl-3-azetidinols.Unhindered amines provide a more facile preparation of derivatives of 1, or its ethers, than do hindered amines, while hindered derivatives of 1 undergo more facile ring closure.
