CAS 1104-49-0

4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid, 6-[[(2-methoxy-1-naphthalenyl)carbonyl]amino]-3,3-dimethyl-7-oxo-, sodiumsalt (1:1), (2S,5R,6R)-

Description:

4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2-methoxy-1-naphthalenyl)carbonyl]amino]-3,3-dimethyl-7-oxo-, sodium salt (1:1), (2S,5R,6R)-, is a complex organic compound characterized by its bicyclic structure, which incorporates both sulfur and nitrogen atoms. This compound features a carboxylic acid functional group, contributing to its acidic properties, and a sodium salt form, which enhances its solubility in aqueous environments. The presence of a methoxy-substituted naphthalene moiety suggests potential aromatic interactions, while the dimethyl and keto groups indicate steric hindrance and reactivity. The stereochemistry, denoted by the (2S,5R,6R) configuration, implies specific spatial arrangements that can influence the compound's biological activity and interactions. This compound may exhibit pharmacological properties, making it of interest in medicinal chemistry. Its unique structural features and functional groups suggest potential applications in drug development or as a biochemical probe, although specific biological activities would require further investigation.

Formula: C₂₀H₂₁N₂NaO₅S

Synonyms:

• 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid, 6-(2-methoxy-1-naphthamido)-3,3-dimethyl-7-oxo-, monosodium salt(7CI,8CI)
• 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,6-[[(2-methoxy-1-naphthalenyl)carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodiumsalt, (2S,5R,6R)- (9CI)
• 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,6-[[(2-methoxy-1-naphthalenyl)carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodiumsalt, [2S-(2a,5a,6b)]-
• Brl 1336
• Nafcillin Desmethyl Impurity

Nafcillin Impurity 4 Sodium Salt

CAS: 1104-49-0

Formula: C₂₀H₁₉N₂O₅S·Na

Molecular weight: 399.45 22.99

Ref: 4Z-N-386

Desmethyl Nafcillin Sodium Salt

Controlled Product

CAS: 1104-49-0

Applications Desmethyl Nafcillin Sodium Salt is derived from (+)-6-Aminopenicillanic Acid (A618895), which is the core structure in penicillins, obtained from the fermentation brew of the Penicillium mold. (+)-6-Aminopenicillanic Acid is used as the main starting block for the preparation of numerous semisynthetic penicillins.
References Zel'tser, I.Z. et al.: Gig. Truda Prof. Zabol., 5, 59 (1983); Hamilton-Miller, J.M.T.: Int. J. Antimicrob. Agents, 31, 189 (2008); Novikova, N.D. et al.: Mikol. Fitopatol., 7, 101 (1973)

Formula: C₂₀H₂₀N₂O₅S·Na

Color and Shape: Neat

Molecular weight: 423.438

Ref: TR-D292740