1353160-88-9 Usage
Uses
Used in Chemical Research:
2-Azetidinepropanoic acid, 2-(Methoxycarbonyl)-1-(phenylMethyl)-, Methyl ester is used as a research compound for studying its chemical properties and potential interactions with other molecules. Its unique structure allows scientists to explore its reactivity and stability, contributing to the understanding of organic chemistry and the development of new synthetic pathways.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Azetidinepropanoic acid, 2-(Methoxycarbonyl)-1-(phenylMethyl)-, Methyl ester is used as a building block for the synthesis of more complex molecules with potential therapeutic applications. Its unique structure and biological activity make it a promising candidate for the development of new drugs targeting various diseases and conditions.
Used in Agrochemical Industry:
2-Azetidinepropanoic acid, 2-(Methoxycarbonyl)-1-(phenylMethyl)-, Methyl ester may also find applications in the agrochemical industry as a precursor for the synthesis of bioactive compounds with potential use in crop protection, pest control, or as plant growth regulators. Its unique structure and potential biological activity can be harnessed to develop novel agrochemicals with improved efficacy and selectivity.
Used in Material Science:
In the field of material science, 2-Azetidinepropanoic acid, 2-(Methoxycarbonyl)-1-(phenylMethyl)-, Methyl ester can be used as a component in the development of new materials with specific properties. Its unique structure and potential for chemical modification make it a valuable building block for the synthesis of polymers, coatings, or other materials with tailored characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1353160-88-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,1,6 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1353160-88:
(9*1)+(8*3)+(7*5)+(6*3)+(5*1)+(4*6)+(3*0)+(2*8)+(1*8)=139
139 % 10 = 9
So 1353160-88-9 is a valid CAS Registry Number.
1353160-88-9Relevant articles and documents
Synthesis of spirocyclopropyl γ-lactams by tandem intramolecular azetidine ring-opening/closing cascade reaction: Synthetic and mechanistic aspects
Nocquet, Pierre-Antoine,Hazelard, Damien,Compain, Philippe
, p. 4117 - 4128 (2012/07/28)
The scope and limitations of a novel intramolecular azetidine ring-opening/closing cascade reaction affording spirocyclopropyl γ-lactams from azetidines in high regio- and stereoselectivity is reported. The key step of the process is a SN2-type ring-opening of TMSOTf-activated azetidine rings by silyl ketene acetals generated by treatment with TMSOTf and TEA. This study is a very rare example of nucleophilic ring-opening of azetidines that does not require formation of quaternary azetidinium salts by N-alkylation or the use of N-electron-withdrawing groups. Application of this process to 2-azetidinone system led to a complete change in reactivity and provide 6-aza-bicyclo[3.2.0]heptane derivatives via an unprecedented Mukaiyama aldol-like reaction involving an ester acceptor and a silyl imidate.
Synthesis of spirocyclopropyl γ-lactams by a highly stereoselective tandem intramolecular azetidine ring-opening/closing cascade reaction
Nocquet, Pierre-Antoine,Hazelard, Damien,Compain, Philippe
scheme or table, p. 6619 - 6623 (2011/12/16)
A new tandem intramolecular azetidine ring-opening/closing cascade reaction affording spirocyclopropyl γ-lactams in high regio-and stereoselectivity is reported. The key step of the process is an SN2-type ring-opening of TMSOTf-activated azetid
