13156-06-4 Usage
Uses
Used in Pharmaceutical Industry:
1-(1-Methylethyl)azetidin-3-ol is used as a building block for the synthesis of pharmaceuticals due to its unique structure and properties. It plays a crucial role in the development of new drugs, enhancing the therapeutic potential and efficacy of various medications.
Used in Agrochemical Industry:
1-(1-Methylethyl)azetidin-3-ol is also used as a building block in the synthesis of agrochemicals, contributing to the development of innovative and effective products for agricultural applications. Its unique properties allow for the creation of new agrochemicals that can improve crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 13156-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,5 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13156-06:
(7*1)+(6*3)+(5*1)+(4*5)+(3*6)+(2*0)+(1*6)=74
74 % 10 = 4
So 13156-06-4 is a valid CAS Registry Number.
13156-06-4Relevant academic research and scientific papers
Facile Syntheses of Azetidin-3-ols by Rearrangement of 2,3-Epoxypropylamines
Oh, Chang Ho,Rhim, Chul Yun,You, Choong Ho,Cho, Jin Rai
, p. 4297 - 4302 (2007/10/03)
The N-alkyl-2,3-epoxypropylamines (2) formed from primary alkylamines (1) and epichlorohydrin were chemoselectively rearranged to the four-membered rings, N-alkylazetidin-3-ols (3), upon treatment of triethylamine in refluxing acetonitrile.
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.
