Nombre del producto:2-Chloro-6-methoxy-3-nitropyridine

IUPAC Name:2-chloro-6-methoxy-3-nitropyridine

CAS:38533-61-8
Fórmula molecular:C6H5ClN2O3
Pureza:97%
Número de catálogo:CM120520
Peso molecular:188.57

Unidad de embalaje Stock disponible Precio($) Cantidad
CM120520-100g in stock Ǫƿ
CM120520-500g in stock ŤǙȃ

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Detalles del producto

Núm. De CAS :38533-61-8
Fórmula molecular:C6H5ClN2O3
Punto de fusión:-
Código de sonrisas:O=[N+](C1=CC=C(OC)N=C1Cl)[O-]
Densidad:
Número de catálogo:CM120520
Peso molecular:188.57
Punto de ebullición:298.5°C at 760 mmHg
Nº Mdl:MFCD00130268
Almacenamiento:Store at room temperature.

Category Infos

Pyridines
Pyridine is a six-membered heterocyclic compound containing one nitrogen heteroatom. Pyridine and piperidine are the most frequently occurring heterocyclic building blocks in drug molecules. According to incomplete statistics, there are currently more than 180 drugs containing pyridine or piperidine structure that have been marketed, nearly 1/5 of the drugs approved for marketing in recent years contain these two structures.
Pyridine | C5H5N | Pyridine Supplier/Distributor/Manufacturer - Chemenu
Pyridine,Pyridine Wholesale,Pyridine for Sale,Pyridine Supplier,Pyridine Distributor,Pyridine Manufacturer
Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell.

Column Infos

Gepotidacin
GSK announces positive headline results from the EAGLE-1 Phase III trial for Gepotidacin in uncomplicated urogenital gonorrhea. Gonorrhoea is the second most common sexually transmitted infection due to the pathogen N. gonorrhoeae. Untreated urogenital gonorrhea can cause serious and permanent health problems, such as pelvic inflammatory disease and infertility.
Gepotidacin is an investigational, first-in-class inhibitor of bacterial topoisomerase. It has a distinct mechanism of action that inhibits bacterial DNA replication by selectively interacting with two key bacterial enzymes, DNA gyrase and topoisomerase IV. Gepotidacin confers activity against most strains of E. coli and S. saprophyticus, and N. gonorrhoeae, including target pathogens resistant to current antibiotics.