1107663-03-5 Usage
Uses
Used in Medicinal Chemistry and Drug Discovery:
Ethyl 2-iodooxazole-4-carboxylate is utilized as a key intermediate in the synthesis of biologically active compounds due to its unique structural features. Its presence in the molecular framework can influence the pharmacological properties of the resulting compounds, making it a valuable asset in the development of new drugs.
Used in Organic Synthesis:
As a building block in organic synthesis, Ethyl 2-iodooxazole-4-carboxylate is employed for the creation of complex organic molecules. Its reactivity allows for the introduction of specific functional groups, which is crucial for the advancement of chemical research and the production of novel materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Ethyl 2-iodooxazole-4-carboxylate is used as a starting material for the development of new drugs. Its unique properties can contribute to the discovery of compounds with improved therapeutic effects and fewer side effects.
Used in Agrochemical Industry:
Ethyl 2-iodooxazole-4-carboxylate also finds applications in the agrochemical industry, where it may be used in the synthesis of new pesticides or other agrochemical products, potentially leading to more effective and environmentally friendly solutions for agricultural challenges.
Used in Material Development:
Ethyl 2-iodooxazole-4-carboxylate's potential in material development is due to its ability to be integrated into the structures of new materials, possibly enhancing their properties or creating materials with unique characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1107663-03-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,7,6,6 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1107663-03:
(9*1)+(8*1)+(7*0)+(6*7)+(5*6)+(4*6)+(3*3)+(2*0)+(1*3)=125
125 % 10 = 5
So 1107663-03-5 is a valid CAS Registry Number.
1107663-03-5Relevant articles and documents
Streamlined Symmetrical Total Synthesis of Disorazole B1and Design, Synthesis, and Biological Investigation of Disorazole Analogues
Aujay, Monette,Dherange, Balu D.,Gavrilyuk, Julia,Gu, Christine,Krieger, Johannes,Lin, Baiwei,Munneke, Stefan,Murhade, Ganesh M.,Nicolaou, K. C.,Purcell, James W.,Sandoval, Joseph,Sarvaiaya, Hetal,Subramanian, Parthasarathi,Vourloumis, Dionisios,Zhang, Zhaomei
supporting information, p. 15476 - 15487 (2020/10/02)
Taking advantage of the C2-symmetry of the antitumor naturally occurring disorazole B1 molecule, a symmetrical total synthesis was devised with a monomeric advanced intermediate as the key building block, whose three-step conversion to the natural product
SUBSTITUTED ARYLOXAZOLES AND THEIR USE
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Page/Page column 24, (2011/06/23)
The present application relates to novel substituted aryloxazole derivatives, a method for the production thereof, the use thereof for the treatment and/or prophylaxis of diseases and the use thereof for the production of drugs for the treatment and/or prophylaxis of diseases, preferably for the treatment and/or prevention of cardiovascular and metabolic disorders.
Total synthesis of enigmazole a from cinachyrella enigmatica. Bidirectional bond constructions with an ambident 2,4-disubstituted oxazole synthon
Skepper, Colin K.,Quach, Tim,Molinski, Tadeusz F.
supporting information; experimental part, p. 10286 - 10292 (2010/09/06)
The first total synthesis of the cytotoxic marine macrolide enigmazole A has been completed in 22 steps (longest linear sequence). The sensitive, densely functionalized 2,4-disubstituted oxazole fragment was constructed using an efficient Negishi-type cou
