913979-70-1 Usage
Uses
Used in Pharmaceutical Industry:
(S)-tert-butyl 2-(2,2,2-trifluoroacetyl)pyrrolidine-1-carboxylate is used as an intermediate in the synthesis of pharmaceuticals for its ability to create diverse structures and properties within organic chemistry. Its unique structure and functional groups contribute to the development of new compounds with specific applications in the medical field.
Used in Agrochemical Industry:
(S)-tert-butyl 2-(2,2,2-trifluoroacetyl)pyrrolidine-1-carboxylate is used as an intermediate in the synthesis of agrochemicals, enabling the creation of new compounds with targeted applications in agriculture. Its unique structure and functional groups play a crucial role in developing effective and innovative products for crop protection and other agricultural uses.
Used in Organic Compounds Synthesis:
(S)-tert-butyl 2-(2,2,2-trifluoroacetyl)pyrrolidine-1-carboxylate is used as a building block in the synthesis of various organic compounds. Its versatility in creating diverse structures and properties makes it an essential component in the development of new and innovative organic compounds for a wide range of applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 913979-70-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,9,7 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 913979-70:
(8*9)+(7*1)+(6*3)+(5*9)+(4*7)+(3*9)+(2*7)+(1*0)=211
211 % 10 = 1
So 913979-70-1 is a valid CAS Registry Number.
913979-70-1Relevant articles and documents
Asymmetric synthesis of (αR)-polyfluoroalkylated prolinols based on the perfluoroalkyl-induced highly stereoselective reduction of perfluoroalkyl n-boc-pyrrolidyl ketones
Funabiki, Kazumasa,Shibata, Akitsugu,Iwata, Hiroki,Hatano, Keisuke,Kubota, Yasuhiro,Komura, Kenichi,Ebihara, Masahiro,Matsui, Masaki
, p. 4694 - 4697 (2008/09/21)
(Chemical Equation Presented) Reduction of the obtained chiral (S)-tert-butyl 2-(perfluoroalkanoyl)pyrrolidine-1-carboxylate with sodium borohydride or lithium aluminum hydride proceeded smoothly to give the corresponding (S)-tert-butyl 2-((R)-perfluoro-1
DIPEPTIDYL PEPTIDASE-IV INHIBITORS
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Page/Page column 135-136, (2008/06/13)
The present invention relates generally to pyrrolidine and thiazolidine DPP-IV inhibitor compounds. The present invention also provides synthetic methods for preparation of such compounds, methods of inhibiting DPP-IV using such compounds and pharmaceutical formulations containing them for treatment of DPP-IV mediated diseases, in particular, Type-2 diabetes.
