(2S,5R)-Benzhydryl 3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4-oxide

• CAT Number: L047213
• CAS Number: 87579-78-0
• Molecular Formula: C21H21NO4S
• Molecular Weight: 383.51
• Purity: ≥95%
• Storage: 2-8°C
• IUPAC Name: benzhydryl (2S,5R)-3,3-dimethyl-4,7-dioxo-4λ4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
• InChI: InChI=1S/C21H21NO4S/c1-21(2)19(22-16(23)13-17(22)27(21)25)20(24)26-18(14-9-5-3-6-10-14)15-11-7-4-8-12-15/h3-12,17-19H,13H2,1-2H3/t17-,19+,27?/m1/s1
• InChIKey: AZIUCAWYSMPKQK-HVHNRQALSA-N
• SMILES: CC1(C(N2C(S1=O)CC2=O)C(=O)OC(C3=CC=CC=C3)C4=CC=CC=C4)C

(2S,5R)-Benzhydryl 3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4-oxide(CAT: L047213) is a complex bicyclic compound that includes a benzhydryl ester, a sulfur atom within the ring structure, and specific stereochemistry at the 2- and 5-positions. This molecule, characterized by its fused 4-thia-1-azabicyclo[3.2.0]heptane core, is significant in pharmaceutical research, particularly in the synthesis of beta-lactam derivatives. Compounds of this type are often investigated for their antibiotic properties, leveraging the beta-lactam core as a structural basis for activity against bacterial cell wall synthesis. (2S,5R)-Benzhydryl 3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4-oxide can serve as a scaffold for developing antibiotics with enhanced resistance to beta-lactamase enzymes, targeting infections more effectively.