6286-51-7 Usage
Description
N-[2-(cyanomethyl)-4,5-dimethoxyphenyl]acetamide is a chemical compound with a molecular formula C13H15N2O3. It is a derivative of acetamide, featuring a cyanomethyl group and dimethoxyphenyl moieties. This versatile compound is known for its potential as a ligand or protein inhibitor in pharmaceutical research and drug development. The cyanomethyl group allows for participation in various chemical reactions, making it a valuable building block in organic synthesis. The dimethoxyphenyl group enhances its bioactivity and potential therapeutic applications, contributing to its pharmacological and biochemical significance.
Uses
Used in Pharmaceutical Research and Drug Development:
N-[2-(cyanomethyl)-4,5-dimethoxyphenyl]acetamide is used as a ligand or protein inhibitor for its potential to modulate biological processes and target specific proteins in the development of new therapeutic agents.
Used in Organic Synthesis:
As a building block in organic synthesis, N-[2-(cyanomethyl)-4,5-dimethoxyphenyl]acetamide is utilized for its ability to participate in various chemical reactions, contributing to the creation of new compounds with potential applications in different fields.
Used in Enhancing Bioactivity and Therapeutic Applications:
The presence of the dimethoxyphenyl group in N-[2-(cyanomethyl)-4,5-dimethoxyphenyl]acetamide is used to increase its bioactivity, making it a promising candidate for the development of drugs with improved efficacy and selectivity in treating various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 6286-51-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6286-51:
(6*6)+(5*2)+(4*8)+(3*6)+(2*5)+(1*1)=107
107 % 10 = 7
So 6286-51-7 is a valid CAS Registry Number.
6286-51-7Relevant articles and documents
Synihesis of 3-substituied indoles via a modified madeling reaction
Orlemans,Schreunder,Conti,Verboom,Reinhoudt
, p. 3817 - 3826 (2007/10/02)
Anilides 4a-c,e-k, lla-d in which the amide function is benzylated, or silylated and having different electron-withdrawing groups (EWG) at the methyl methyl in the ortho position of the amide function, cyclize under the influence of potassium tert-butoxide to the corresponding indole derivatives 5a-c,e-k and 9a-d, respectively, under these conditions the chloroacetamides 4d,n and 11e are converted into the tetrahydroquinolines 6a,b and 12, respectively. Treatment of chloroacetamide 4m with KOt-Bu gave, in addition to starting material, indole 5m, tetrahydroquinoline 6c and 2(1H)-quinolinone 7. When 3-indolecarbonitrile 5a is treated with sodium in liquid amnonia debenzylation takes place, while after catalytic hydrogenation with 5% Pd/C the corresponding 2,3-dirnethylindole 8 is formed.
