652158-82-2 Usage
Uses
Used in Pharmaceutical Development:
Ethyl 5-(2-(tert-butoxycarbonylamino)ethyl)-1,2,4-oxadiazole-3-carboxylate is used as a key intermediate in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs with diverse therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, ethyl 5-(2-(tert-butoxycarbonylamino)ethyl)-1,2,4-oxadiazole-3-carboxylate is used as a building block or a reagent to construct complex organic molecules, taking advantage of its reactive functional groups.
Used in Medicinal Chemistry:
Ethyl 5-(2-(tert-butoxycarbonylamino)ethyl)-1,2,4-oxadiazole-3-carboxylate is employed as a component in the design and synthesis of biologically active compounds, leveraging its potential antimicrobial and anti-inflammatory properties for therapeutic applications.
Used in Peptide Synthesis:
In peptide synthesis, ethyl 5-(2-(tert-butoxycarbonylamino)ethyl)-1,2,4-oxadiazole-3-carboxylate is used as a protecting group for amine groups, preventing unwanted side reactions and facilitating the controlled formation of peptide bonds.
Used in Drug Discovery:
Ethyl 5-(2-(tert-butoxycarbonylamino)ethyl)-1,2,4-oxadiazole-3-carboxylate is utilized in drug discovery processes to explore its potential as a lead compound or to modify existing drug candidates, enhancing their efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 652158-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,2,1,5 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 652158-82:
(8*6)+(7*5)+(6*2)+(5*1)+(4*5)+(3*8)+(2*8)+(1*2)=162
162 % 10 = 2
So 652158-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H19N3O5/c1-5-18-10(16)9-14-8(20-15-9)6-7-13-11(17)19-12(2,3)4/h5-7H2,1-4H3,(H,13,17)
652158-82-2Relevant academic research and scientific papers
CARBOXAMIDE DERIVATIVE
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Page/Page column 64, (2010/11/08)
An SGLT inhibitor comprising a compound of the formula: (|) wherein the ring A is an optionally substituted ring; R1 is an optionally substituted hydrocarbon group, etc.; each of R2 and R3 independently is a hydrogen atom, an optionally substituted hydrocarbon group, etc.; R4 is an optionally substituted hydrocarbon group, etc.; and X is a bivalent chain group whose main chain consists of 1 to 6 atoms. This SGLT inhibitor is useful as a preventive/therapeutic agent for diabetes mellitus, obesity, hypertension, hyperlipemia, etc.
Large scale synthesis of 1,2,4- and 1,3,4-oxadiazole carboxylates
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Page 5, (2008/06/13)
Disclosed are efficient and scalable processes for preparing 1,2,4- and 1,3,4-oxadiazole carboxylates from readily available starting materials.
