433267-56-2 Usage
Uses
Used in Pharmaceutical Synthesis:
Ethyl 4-iodo-1H-pyrrole-2-carboxylate is used as a key building block for the synthesis of various pharmaceuticals. Its presence of an iodine atom and functional groups allows for further chemical reactions, making it a versatile component in the development of new drugs.
Used in Organic Chemistry:
In the field of organic chemistry, Ethyl 4-iodo-1H-pyrrole-2-carboxylate is utilized as a reagent or intermediate in the preparation of complex organic molecules. Its unique structure facilitates specific types of chemical reactions, contributing to the advancement of organic synthesis techniques.
Used in Bioactive Compound Production:
Ethyl 4-iodo-1H-pyrrole-2-carboxylate is employed as a precursor in the production of bioactive compounds. Its ability to participate in various chemical transformations makes it instrumental in the creation of molecules with potential biological activity, which can be further explored for therapeutic applications.
Used in Organic Material Development:
Ethyl 4-iodo-1H-pyrrole-2-carboxylate is also used in the development of organic materials, where its structural and reactive properties are leveraged to create new materials with specific properties for various applications, such as in electronics or as specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 433267-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,3,2,6 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 433267-56:
(8*4)+(7*3)+(6*3)+(5*2)+(4*6)+(3*7)+(2*5)+(1*6)=142
142 % 10 = 2
So 433267-56-2 is a valid CAS Registry Number.
433267-56-2Relevant academic research and scientific papers
Traceless linking of pyrroles: General methology and solid phase supported functionalizations
Bergauer, Markus,Gmeiner, Peter
, p. 274 - 278 (2007/10/03)
Transacetalization reaction of the diethoxymethyl (DEM) protected pyrroles 2a-f with the diol functionalized resin 3 resulted in the formation of the immobilized pyrroles 4a-f. Regioselective transformations including Pd-catalyzed coupling reactions and reductive aminations on solid phase were demonstrated.
