35848-07-8 Usage
Uses
Used in Pharmaceutical Industry:
(R)-2-Methylazetidine is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form different types of chemical bonds, contributing to the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
(R)-2-Methylazetidine is utilized as a building block in the production of agrochemicals, enabling the creation of novel compounds with potential applications in crop protection and pest control.
Used in Fine Chemicals Industry:
(R)-2-Methylazetidine is employed as a versatile intermediate in the synthesis of fine chemicals, including specialty chemicals and advanced materials, due to its unique reactivity and structural properties.
Used in Drug Discovery and Development:
(R)-2-Methylazetidine is used as a valuable compound in drug discovery and development, where its unique structure and reactivity can lead to the creation of innovative therapeutic agents with enhanced properties.
Used in Asymmetric Catalysis:
(R)-2-Methylazetidine is applied in asymmetric catalysis as a key component for the creation of molecules with specific stereochemistry, which is crucial for the development of enantiomerically pure compounds with desired biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 35848-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,4 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35848-07:
(7*3)+(6*5)+(5*8)+(4*4)+(3*8)+(2*0)+(1*7)=138
138 % 10 = 8
So 35848-07-8 is a valid CAS Registry Number.
35848-07-8Relevant academic research and scientific papers
Lithiation-electrophilic substitution of N-thiopivaloylazetidine
Hodgson, David M.,Kloesges, Johannes
supporting information; experimental part, p. 2900 - 2903 (2010/06/19)
(Figure Presented) The fourth protocol: The rarely studied Nthiopivaloyl group plays a crucial role in mediating efficient ∞ lithiation and incorporation of diverse electrophiles onto an azetidine ring; in the presence of chiral ligands, this chemistry also provides the first example of an enantioselective electrophilic substitution on a four-membered ring.
Conformational and chiroptical properties of N-nitrosoazetidines
Shustov,Rauk
, p. 928 - 934 (2007/10/02)
Optically active N-nitrosoazetidines, containing the isolated nitrosoazetidine chromophore, i.e. (2R)-1-nitroso-2-methylazetidine (2) and (4S)-1-nitroso-2,2-dibutyl-4-methylazetidine (5), are synthesized, and their 1H NMR, CD, and UV spectra ar
