CAS 6456-44-6
:Pyridinium, 3-(aminocarbonyl)-1-methyl-, iodide (1:1)
Description:
Pyridinium, 3-(aminocarbonyl)-1-methyl-, iodide (1:1), commonly referred to as a pyridinium salt, is a quaternary ammonium compound characterized by its pyridine ring structure substituted with an aminocarbonyl group and a methyl group. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols due to its ionic nature. The presence of the iodide ion contributes to its solubility and can influence its reactivity and stability. Pyridinium salts are known for their ability to act as strong electrophiles, making them useful in various organic synthesis reactions. Additionally, the aminocarbonyl group can participate in hydrogen bonding, enhancing the compound's interactions with other molecules. The compound's properties, including melting point, boiling point, and reactivity, can vary based on environmental conditions and the presence of other chemical species. Overall, this substance is of interest in both synthetic organic chemistry and potential applications in pharmaceuticals.
Formula:C7H9N2O·I
InChI:InChI=1S/C7H8N2O.HI/c1-9-4-2-3-6(5-9)7(8)10;/h2-5H,1H3,(H-,8,10);1H
InChI key:InChIKey=IWEIZMCTGMHCRE-UHFFFAOYSA-N
SMILES:C(N)(=O)C1=C[N+](C)=CC=C1.[I-]
Synonyms:- 3-(Aminocarbonyl)-1-methylpyridinium iodide
- 3-Carbamoyl-1-Methylpyridinium
- 3-Carbamoyl-1-methylpyridinium iodide
- N'-{3-[(2,3-dihydro-1H-inden-5-yloxy)methyl]benzoyl}-2,6-dimethoxybenzohydrazide
- Nicotinamide methiodide
- Nsc 23359
- Pyridinium, 3-(aminocarbonyl)-1-methyl-, iodide
- Pyridinium, 3-(aminocarbonyl)-1-methyl-, iodide (1:1)
- Pyridinium, 3-carbamoyl-1-methyl-, iodide
- Pyridinium, 3-carbamoyl-1-methyl-, iodide (8CI)
- Pyridinium, 3-carbamyl-1-methyl-, iodide
- 1-Methylnicotinamide iodide
- 3-(aminocarbonyl)-1-methylpyridiniumiodide
- 1-methylpyridine-5-carboxamide iodide
- 1-Methyl-3-carbamoylpyridinium·iodide
- nicotinamidemethiodide
- N-METHYLNICOTINAMIDE IODIDE
- 1-METHYLNICOTINAMIDE IODIDE SALT
- 1-METHYL-NICOTINAMIDE IODIDE
- 3-carbamoyl-1-methylpyridiniumiodide
- 3-(aminocarbonyl)-1-methyl-pyridiniuiodide
- LABOTEST-BB LT00233117
- N-METHYLNICOTINIC ACID AMIDE IODIDE SALT
- See more synonyms
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Found 11 products.
4-Iodo-1-methyl-1,2-dihydropyridine-3-carboxamide
CAS:Formula:C7H9IN2OPurity:98%Color and Shape:SolidMolecular weight:264.06361-Methylnicotinamide-13C-d3 Iodide
CAS:Formula:C613CH6D3N2O·IColor and Shape:Pale Yellow SolidMolecular weight:141.17 126.913-Carbamoyl-1-methylpyridin-1-ium iodide
CAS:3-Carbamoyl-1-methylpyridin-1-ium iodidePurity:98%Molecular weight:264.06g/mol1-Methylnicotinamide Iodide
CAS:Formula:C7H9N2O·IColor and Shape:Pale Yellow SolidMolecular weight:137.16 126.911-Methylnicotinamide Iodide
CAS:Controlled ProductFormula:C7H9N2O·IColor and Shape:NeatMolecular weight:264.061-Methyl-nicotinamide Iodide
CAS:Controlled Product<p>Applications A nicotinic acid derivative which shows a dopaminergic neurotoxicity.<br>References Rollema, H., et al.: J. Med. Chem., 33, 2221 (1990),<br></p>Formula:C7H9IN2OColor and Shape:NeatMolecular weight:264.061-Methylnicotinamide-d3 Iodide
CAS:Controlled Product<p>Applications 3-(Aminocarbonyl)-1-methylpyridinium-d3 Iodide is the isotope labelled derivative of 1-Methylnicotinamide (M323235), a nicotinic acid derivative which shows a dopaminergic neurotoxicity.<br>References Rollema, H., et al.: J. Med. Chem., 33, 2221 (1990),<br></p>Formula:C7H6D3IN2OColor and Shape:Light YellowMolecular weight:267.081-Methyl-nicotinamide iodide
CAS:<p>1-Methyl-nicotinamide iodide is a drug that has been used in clinical trials for the treatment of type 2 diabetes mellitus. It is thought to work by increasing the sensitivity of cells to insulin, which may be related to its ability to bind to protein amide groups and form hydrogen bonds with the amino acid side chains. The compound also has been shown to increase the activity of the enzyme glycogen synthase in rats. 1-Methyl-nicotinamide iodide is soluble in water and human serum, and shows low solubility in ethanol. It has not been studied in humans, but animal studies have shown that it can be absorbed orally and metabolized into hippuric acid, which is excreted as a metabolic product through urine. Animal studies also showed that 1-methyl-nicotinamide iodide inhibits glucose production by pancreatic beta cells, which may lead to an increased insulin response after eating.</p>Formula:C7H9IN2OPurity:Min. 95%Color and Shape:Off-White PowderMolecular weight:264.06 g/mol3-Carbamoyl-1-methylpyridin-1-ium iodide monohydrate
CAS:Formula:C7H9IN2OPurity:96%Molecular weight:264.066







