54916-65-3 Usage
General Description
5-Chloro-2-methoxynicotinic acid is a chemical compound with the molecular formula C7H6ClNO3. It is a derivative of nicotinic acid and contains a chlorine atom and a methoxy group attached to the 5 and 2 positions respectively on the nicotinic acid ring. 5-Chloro-2-methoxynicotinic acid has potential applications in the fields of pharmaceuticals, agrochemicals, and materials science due to its unique structure and properties. It may be used as a building block in the synthesis of various organic compounds and can also be utilized in the development of new drugs or agrochemicals. Moreover, 5-chloro-2-methoxynicotinic acid may also have potential uses in the production of advanced materials and in research and development efforts. Further studies and applications of this chemical compound are ongoing, and its potential uses and properties continue to be explored.
Check Digit Verification of cas no
The CAS Registry Mumber 54916-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,1 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54916-65:
(7*5)+(6*4)+(5*9)+(4*1)+(3*6)+(2*6)+(1*5)=143
143 % 10 = 3
So 54916-65-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClNO3/c1-12-6-5(7(10)11)2-4(8)3-9-6/h2-3H,1H3,(H,10,11)
54916-65-3Relevant articles and documents
Spiro hydantoin aldose reductase inhibitors derived from 8-aza-4-chromanones
Sarges,Goldstein,Welch,Swindell,Siegel,Beyer
, p. 1859 - 1865 (2007/10/02)
A series of spiro hydantoins derived from 8-azachromanones (2,3-dihydro-4H-pyrano[2,3-b]pyridin-4-ones) has been prepared and tested for aldose reductase inhibitory activity. The standard Bucherer-Bergs conditions had to be drastically modified to increas
AN IMPROVED METHOD OF CHLORINATING 2-ALKOXYNICOTINIC ACIDS
Elliott, Mark L.,Goddard, Carl J.
, p. 1505 - 1508 (2007/10/02)
A novel chlorination process for preparing 5-chloro-2-alkoxynicotinic acids has been developed using commercial 5.25percent sodium hypochlorite (Clorox) as a chlorinating agent.
Chlorination of 2-methoxynicotinic acid
-
, (2008/06/13)
A novel process for chlorinating 2-methoxynicotinic acid at the 5-position of the molecule is disclosed. The process involves the use of an alkali metal hypochlorite as the chlorinating agent in a homogeneous aqueous solvent system. The compound so produced, 5-chloro-2-methoxynicotinic acid, is known to be useful as an intermediate leading to various oral hypoglycemic agents of the benzenesulfonylurea class.
