3569-99-1 Usage
Description
3-Pyridinecarboxylic acid N-hydroxymethylamide, also known as N-(hydroxymethyl)nicotinamide, is a white solid with antimicrobial properties. It is a decomposition product found in the preparation of Nicotinic acid and has been reported for quantitative determination in tablets and basic solutions by thin-layer chromatography-densitometric methods.
Uses
Used in Pharmaceutical Industry:
3-Pyridinecarboxylic acid N-hydroxymethylamide is used as a cholagogue agent for the treatment of various digestive disorders. It aids in the secretion of bile from the liver, which is essential for the digestion and absorption of fats and fat-soluble vitamins.
Used in Chemical Industry:
3-Pyridinecarboxylic acid N-hydroxymethylamide is used as a decomposition product in the preparation of Nicotinic acid, which is an essential component in the synthesis of various pharmaceuticals and chemicals.
Used in Antimicrobial Applications:
As an antimicrobial agent, 3-Pyridinecarboxylic acid N-hydroxymethylamide is employed in the development of products that help prevent the growth of harmful microorganisms, thereby maintaining cleanliness and hygiene in various settings.
Used in Research and Development:
3-Pyridinecarboxylic acid N-hydroxymethylamide is utilized in research and development for the study of its chemical properties, potential applications, and possible integration into new products and formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 3569-99-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,6 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3569-99:
(6*3)+(5*5)+(4*6)+(3*9)+(2*9)+(1*9)=121
121 % 10 = 1
So 3569-99-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2/c10-5-9-7(11)6-2-1-3-8-4-6/h1-4,10H,5H2,(H,9,11)
3569-99-1Relevant articles and documents
3D, 2D and 1D networks via N-H... O and N-H... N hydrogen bonding by the bis-amide analogues: Effect of chain lengths and odd-even spacers
Mukherjee, Gargi,Biradha, Kumar
, p. 1285 - 1290 (2014)
The synthesis, crystal structures and hydrogen bonding networks of four members of the bis(pyridinecarboxamido)alkane and bis(pyridyl)alkanediamides series (1 ≈ n ; 8), where the amide moieties are separated by alkyl chain (-(CH2)n-) having even or odd number of -(CH2)-groups are explored and correlated with the previously reported structures. The odd members (n = odd) of both the series are found to adopt three-dimensional networks in contrast to the 1D or 2D structures of the even members (n = even). This odd-even effect on the dimensionality of the networks however disappears with increase in chain length.
Synthesis, characterization and biological activity of 1,3,4-substituted 2-azetidinones
Pandey,Gupta,Upadhyay, Mrinalini,Upadhyay, Mridula,Singh,Tandon, Meenal
, p. 158 - 162 (2007/10/03)
Amido/imido alcohol/2-phenyl-3-hydroxyethylquinazolin-4 (3H) -one 1 on treatment with benzoic acid in the presence of cone. H2SO4 yields m-(aralkylamido/imidoalkyl/2-phenyl-3-ethyl-3H-4-oxoquinazolinyl) benzoic acids 2. The acid chloride of 2 on reaction with hydrazine hydrate affords m-(aralkylamido/imidoalkyl/2-phenyl-3-ethyl-3H-4-oxo-quinazolinyl) benzoic acid hydrazides 4 which on condensation with an aromatic aldehyde in acetic acid gives m-(aralkylamido/imidoalkyl/2-phenyl-3-ethyl-3H-4-oxo- quinazolinyl) benzoic acid hydrazones 5. Compounds 5 undergo cyclization with phenoxy acetic acid in the presence of thionyl chloride in dry benzene to furnish 1-[m-(aralkylamido/imidoalkyl/2-phenyl-3-ethyl-3H-4-oxo-quinazolinyl- benzamido)]-3-phenoxy-4-phenyl-2-azetidinones 6. The antiviral and antifungal activities of 6 have been reported.
