470690-99-4 Usage
Description
[2-MERCAPTO-3-(4-METHOXY-BENZYL)-3H-IMIDAZOL-4-YL]-METHANOL is a chemical compound with the molecular formula C12H14N2O2S. It is a derivative of the imidazole ring, featuring a mercapto group (SH) and a methoxybenzyl group. This unique structure and the presence of functional groups suggest potential applications in various fields, including pharmaceuticals and industrial processes. It may serve as a building block for the synthesis of new drug compounds or act as a catalyst in chemical reactions. Further research and testing are necessary to explore its full potential and properties.
Uses
Used in Pharmaceutical Industry:
[2-MERCAPTO-3-(4-METHOXY-BENZYL)-3H-IMIDAZOL-4-YL]-METHANOL is used as a building block for the synthesis of new drug compounds due to its unique imidazole ring structure and functional groups, which can be exploited for the development of novel therapeutic agents.
Used in Chemical Industry:
In the chemical industry, [2-MERCAPTO-3-(4-METHOXY-BENZYL)-3H-IMIDAZOL-4-YL]-METHANOL may be utilized as a catalyst in various chemical reactions, taking advantage of its reactive mercapto group and other functional moieties to facilitate or enhance specific transformations.
Further research and development are required to fully understand the potential applications and benefits of [2-MERCAPTO-3-(4-METHOXY-BENZYL)-3H-IMIDAZOL-4-YL]-METHANOL in these industries and to optimize its use in practical settings.
Check Digit Verification of cas no
The CAS Registry Mumber 470690-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,0,6,9 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 470690-99:
(8*4)+(7*7)+(6*0)+(5*6)+(4*9)+(3*0)+(2*9)+(1*9)=174
174 % 10 = 4
So 470690-99-4 is a valid CAS Registry Number.
470690-99-4Relevant articles and documents
Preparation of a clinically investigated ras farnesyl transferase inhibitor
Maligres, Peter E.,Waters, Marjorie S.,Weissman, Steven A.,McWilliams, J. Christopher,Lewis, Stephanie,Cowen, Jennifer,Reamer, Robert A.,Volante,Reider, Paul J.,Askin, David
, p. 229 - 241 (2007/10/03)
The synthesis of ras farnesyl-protein transferase inhibitor 1 is described on a multi-kilogram scale. Retrosynthetic analysis reveals chloromethylimidazole 2 and a piperazinone 3 as viable precursors. The 1,5-disubstituted imidazole system was regioselectively assembled via an improved Marckwald imidazole synthesis. A new imidazole dethionation procedure has been developed to convert the Marckwald mercaptoimidazole product to the desired imidazole. This methodology was found to be tolerant of a variety of functional groups providing good to excellent yields of 1,5-disubstituted imidazoles. A new Mitsunobu cyclization strategy was developed to prepare the arylpiperazinone fragment 3.
