111043-48-2 Usage
Uses
Used in Industrial and Manufacturing Processes:
1-Methyl-3-azetidinol is used as a solvent for its ability to dissolve a variety of substances, facilitating processes in different industries.
Used in Organic Synthesis:
1-Methyl-3-azetidinol serves as a reagent in organic synthesis, contributing to the formation of complex organic compounds through chemical reactions.
Used in Pharmaceutical Production:
1-Methyl-3-azetidinol is utilized in the production of pharmaceuticals, playing a role in the synthesis of various medicinal compounds.
Used in Agrochemical Production:
1-Methyl-3-azetidinol is also used in the production of agrochemicals, indicating its application in the agricultural sector for the development of products that protect and enhance crop yields.
While the specific applications in different industries are not detailed in the provided materials, the general uses of 1-Methyl-3-azetidinol are outlined above, highlighting its versatility and importance in a range of chemical and manufacturing processes.
Check Digit Verification of cas no
The CAS Registry Mumber 111043-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,4 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 111043-48:
(8*1)+(7*1)+(6*1)+(5*0)+(4*4)+(3*3)+(2*4)+(1*8)=62
62 % 10 = 2
So 111043-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO/c1-5-2-4(6)3-5/h4,6H,2-3H2,1H3
111043-48-2Relevant academic research and scientific papers
THIAZOLIDINONE COMPOUNDS AND USE THEREOF
-
Paragraph 1062-1063, (2017/09/21)
A pharmaceutical composition containing a compound of Formula (I) for treating an opioid receptor-associated condition. Also disclosed is a method for treating an opioid receptor-associated condition using such a compound. Further disclosed are two sets of thiazolidinone compounds of formula (I): (i) compounds each having an enantiomeric excess greater than 90% and (ii) compounds each being substituted with deuterium.
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.
