Nom du produit:sodium (6R,7R)-7-(2-(3,5-dichloro-4-oxopyridin-1(4H)-yl)acetamido)-3-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
IUPAC Name:sodium (6R,7R)-7-[2-(3,5-dichloro-4-oxo-1,4-dihydropyridin-1-yl)acetamido]-3-{[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
- CAS：63521-15-3
- Formule moléculaire：C18H14Cl2N5NaO5S3
- Pureté：97%
- Numéro de catalogue：CM176271
- Poids moléculaire：570.41
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Détails du produit
- N° CAS:63521-15-3
- Formule moléculaire:C18H14Cl2N5NaO5S3
- Point de fusion:-
- Code SMILES:O=C(C(N12)=C(CSC3=NN=C(C)S3)CS[C@]2([H])[C@H](NC(CN(C=C4Cl)C=C(Cl)C4=O)=O)C1=O)[O-].[Na+]
- Densité:
- Numéro de catalogue:CM176271
- Poids moléculaire:570.41
- Point d'ébullition:
- N° Mdl:
- Stockage:
Category Infos
- Azetidines
- Azetidines are an important class of saturated four-membered nitrogen-containing heterocyclic compounds. The research hotspots related to this structure mainly focus on two aspects: one is the research of pharmaceutical chemistry; the other is related to chiral azetidines, using rigid azetidine compounds as chiral ligands for asymmetric catalytic reactions. Many nitrogen-containing heterocycles play important roles in drug structures, and in many cases small structural changes can improve ligand selectivity and pharmacokinetic properties.
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- Thiazines
- Thiazine is an organic compound containing four carbon rings, one nitrogen atom and one sulfur atom. Thiazine has three isomers, 1,2-thiazine, 1,3-thiazine and 1,4-thiazine, which are arranged differently in the ring. Nitrogen-containing heterocyclic compounds such as 1,4-thiazine and its benzo derivatives are important compounds in many different research fields due to their remarkable biological properties.
- Thiadiazoles
- Thiadiazoles are a subfamily of azoles. Structurally, they are five-membered heterocyclic compounds containing two nitrogen atoms and one sulfur atom, and two double bonds, forming an aromatic ring. Depending on the relative positions of the heteroatoms, there are four possible structures; these forms do not interconvert and are therefore structural isomers rather than tautomers. These compounds themselves are rarely synthesized and have no particular utility, however, compounds that use them as structural motifs are fairly common in pharmacology.
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