53171-35-0 Usage
Uses
Used in Pharmaceutical Industry:
SUCCINAMIC ACID ETHYL ESTER is used as a solvent, intermediate, and additive for the synthesis of pharmaceuticals. Its properties make it suitable for use in the development of various medications, contributing to the production process of drugs.
Used in Agrochemical Industry:
In the agrochemical sector, SUCCINAMIC ACID ETHYL ESTER serves as a key intermediate in the synthesis of various agrochemicals. Its role in this industry is crucial for the production of compounds that protect crops and enhance agricultural productivity.
Used in Organic Compounds Synthesis:
SUCCINAMIC ACID ETHYL ESTER is utilized as an intermediate in the synthesis of other organic compounds. Its reactivity and stability make it a valuable component in creating a wide range of organic chemicals for different applications.
Used in Research Applications:
As a versatile chemical, SUCCINAMIC ACID ETHYL ESTER is also used in research settings. Its properties allow scientists to explore its potential uses and reactions in various chemical and biological studies, further expanding its applications and understanding of its capabilities.
Check Digit Verification of cas no
The CAS Registry Mumber 53171-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,7 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53171-35:
(7*5)+(6*3)+(5*1)+(4*7)+(3*1)+(2*3)+(1*5)=100
100 % 10 = 0
So 53171-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO3/c1-2-10-6(9)4-3-5(7)8/h2-4H2,1H3,(H2,7,8)
53171-35-0Relevant academic research and scientific papers
EIF4E INHIBITORS AND USES THEREOF
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Paragraph 00334, (2020/03/29)
The present invention provides compounds inhibiting elF4E activity, and compositions and methods of using thereof. Compounds of the present invention, and pharmaceutically acceptable compositions thereof, are useful for treating a variety of diseases, dis
Reaction of γ-dicarboxylic acids amides and imides with trifluoromethanesulfonamide and formaldehyde
Moskalik,Meshcheryakov,Shainyan
body text, p. 1644 - 1650 (2010/04/27)
Three-component condensation of trifluoromethanesulfonamide with paraformaldehyde and succinamide depending on the reaction conditions led alongside bis(trifluoromethanesulfonamido)methane to the formation of a substitution product, bis[(trifluoromethylsulfonyl)aminomethyl]succinamide, or to a cyclization product, N-[trifluoromethylsulfonyl)aminomethyl]succinimide. The attempt to obtain the latter by the reaction of the trifluoromethanesulfonamide sodium salt CF3SO2NHNa with N-chloromethylsuccinimide unexpectedly resulted in N,N-bis(succinimidomethyl)-trifluoromethanesulfonamide. Analogously the reaction of CF3SO2NHNa with N-chloromethyl-phthalimide gave N,N-bis(phthalimidomethyl)trifluoromethanesulfonamide. The reaction of CF3SO2NHNa with succinimide and phthalimide in water and alcohol solution resulted in the ring opening and further transformation of the formed monosubstituted N-(trifluoromethylsulfonyl)amides of succinic and phthalic acids.
