1107663-03-5 Usage
General Description
Ethyl 2-iodooxazole-4-carboxylate is a chemical compound with the molecular formula C6H6INO3. Ethyl 2-iodooxazole-4-carboxylate is a derivative of oxazole, a five-membered aromatic heterocycle containing one oxygen and one nitrogen atom in the ring. The presence of the ethyl ester and iodine moiety in the structure makes it a versatile building block for organic synthesis, particularly in the field of medicinal chemistry and drug discovery. It can be used as a starting material for the synthesis of various biologically active compounds, and its reactivity can be harnessed for the introduction of specific functional groups into organic molecules. The compound is also of interest in the development of new materials and has potential applications in the pharmaceutical and agrochemical industries.
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
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
