10177-32-9 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 4-methoxynicotinate is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Cardiovascular Disease Treatment:
Methyl 4-methoxynicotinate is used as a vasodilator for its capacity to improve blood flow and potentially treat cardiovascular diseases by reducing the strain on the heart.
Used in Inflammatory Condition Treatment:
Due to its anti-inflammatory properties, Methyl 4-methoxynicotinate is used in the treatment of inflammatory conditions to alleviate symptoms and reduce inflammation.
Used in Medicinal Chemistry and Drug Development:
Methyl 4-methoxynicotinate is used as a compound of interest in medicinal chemistry and drug development for its antioxidant and neuroprotective effects, which may contribute to the development of treatments for neurodegenerative diseases and other conditions where oxidative stress plays a role.
Check Digit Verification of cas no
The CAS Registry Mumber 10177-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,7 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10177-32:
(7*1)+(6*0)+(5*1)+(4*7)+(3*7)+(2*3)+(1*2)=69
69 % 10 = 9
So 10177-32-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO3/c1-11-7-3-4-9-5-6(7)8(10)12-2/h3-5H,1-2H3
10177-32-9Relevant articles and documents
The Reaction of N -Trimethylsilyl-Substituted Heteroarylamines with Esters and Thioesters: An Efficient Protocol to Access Diheteroarylamides
Koperniku, Ana,Zamiri, Maryam,Grierson, David S.
, p. 1779 - 1790 (2019)
The S -benzyl thioester and methyl ester derivatives of a representative 4-pyridinone-based carboxylic acid were sufficiently activated to react efficiently in amide coupling reactions with the amide anion generated in situ from the N -trimethylsilyl derivative of different weakly nucleophilic heteroarylamines. In acetonitrile as solvent, the precipitated diheteroarylamide products were isolated in pure form by vacuum filtration. This simple amide bond forming protocol can be readily adapted to the parallel synthesis of compound libraries.
Syntheses of ortho-hydroxymethylpyridinols and dioxaphosphorino[m,n-x]pyridines
Leroy,Despres,Bigan,Blondeau
, p. 2257 - 2272 (2007/10/03)
Dioxaphosphorino[m,n-x]pyridines compounds have been prepared by condensation of methyl dichlorophosphate with new ortho-hydroxymethylpyridinols.
