756813-88-4 Usage
Uses
Used in Pharmaceutical Research:
Methyl 2-(4-amino-3-iodophenyl)-2-methylpropanoate is used as a building block in pharmaceutical research for the preparation of various pharmaceuticals and bioactive molecules. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, Methyl 2-(4-amino-3-iodophenyl)-2-methylpropanoate is utilized as a reagent in chemical reactions. Its presence can facilitate the formation of desired products, contributing to the advancement of organic chemistry.
Used in Synthesis of Complex Organic Compounds:
Methyl 2-(4-amino-3-iodophenyl)-2-methylpropanoate also serves as a precursor in the synthesis of complex organic compounds. Its involvement in these processes can lead to the creation of intricate molecules with specific properties and applications.
Used in Chemical Reactions:
As a reagent, Methyl 2-(4-amino-3-iodophenyl)-2-methylpropanoate is used in various chemical reactions to achieve specific outcomes. Its participation in these reactions can lead to the formation of new compounds or the modification of existing ones, expanding the scope of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 756813-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,6,8,1 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 756813-88:
(8*7)+(7*5)+(6*6)+(5*8)+(4*1)+(3*3)+(2*8)+(1*8)=204
204 % 10 = 4
So 756813-88-4 is a valid CAS Registry Number.
756813-88-4Relevant academic research and scientific papers
Farr, Roger N.,Alabaster, Ramon J.,Chung, John Y.L.,Craig, Bridgette,Edwards, John S.,Gibson, Andrew W.,Ho, Guo-Jie,Humphrey, Guy R.,Johnson, Simon A.,Grabowski
, p. 3503 - 3515 (2003)
An efficient, high yield process for the synthesis of a GnRH antagonist has been developed. We have demonstrated that under boron trifluoride mediation, nosyl aziridines will react with 2-arylindole derivatives to afford β-substituted tryptamines in an enantiospecific process with remarkably high regioselectivity. The scope of the reaction was explored with several 2-substituted nosyl aziridines. The key reaction was developed expressly for the GnRH antagonist program and has been demonstrated on 40 kilogram scale.
