CAS 5657-61-4
:Nicotinohydroxamic acid
Description:
Nicotinohydroxamic acid, with the CAS number 5657-61-4, is a chemical compound that features a pyridine ring, characteristic of nicotinic derivatives, combined with a hydroxamic acid functional group. This compound is known for its potential applications in medicinal chemistry, particularly as a precursor in the synthesis of various pharmaceuticals. It exhibits properties typical of hydroxamic acids, such as the ability to chelate metal ions, which can influence biological activity and reactivity. The presence of the pyridine moiety contributes to its polar nature, enhancing solubility in polar solvents. Additionally, nicotinohydroxamic acid may exhibit biological activities, including antimicrobial and anti-inflammatory properties, making it of interest in drug development. Its stability and reactivity can be influenced by pH and the presence of other functional groups in a reaction environment. Overall, nicotinohydroxamic acid represents a versatile compound with significant potential in both research and therapeutic applications.
Formula:C6H6N2O2
InChI:InChI=1S/C6H6N2O2/c9-6(8-10)5-2-1-3-7-4-5/h1-4,10H,(H,8,9)
InChI key:InChIKey=IYCHDNQCHLMLJZ-UHFFFAOYSA-N
SMILES:C(NO)(=O)C=1C=CC=NC1
Synonyms:- Nicotinohydroximic acid
- Nicotinohydroxamic acid
- Nicoxamat
- Nicotinylhydroxamic acid
- Nicotinylhydroxamic acid
- N-Hydroxy-3-pyridinecarboxamide
- 3-Pyridinecarboxamide, N-hydroxy-
- Nicotinohydroxamic acid
- 3-Pyridinecarbohydroxamic acid
- N-hydroxypyridine-3-carboxamide
- Nicotinohydroximic acid
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
N-Hydroxypyridine-3-carboxamide
CAS:N-Hydroxypyridine-3-carboxamide is a hydroxylated metabolite of nicotinic acid that has been shown to have skin conditioning properties. The optimum pH for this product is 3.5 and its biological properties include an inhibitory effect on viral replication and a galacturonic acid complex. N-Hydroxypyridine-3-carboxamide also exhibits a high degree of hemolytic activity, which may be due to the methyl nicotinate moiety or the carbonyl oxygens present in this compound.
Formula:C6H6N2O2Purity:Min. 95%Molecular weight:138.12 g/mol



