(2S,5R)-6,6-Dibromo-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide

Reagent Code: #232758
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CAS Number 76646-91-8

science Other reagents with same CAS 76646-91-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 391.03 g/mol
Formula C₈H₉Br₂NO₅S
badge Registry Numbers
MDL Number MFCD28137728
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Widely used in the pharmaceutical industry as an intermediate in the synthesis of carbapenem antibiotics. These antibiotics are known for their broad-spectrum activity and resistance to beta-lactamases, making them effective against multidrug-resistant bacterial infections. The compound's structure enables enhanced stability and reactivity in forming key beta-lactam ring systems essential for antimicrobial activity. It plays a critical role in producing potent antibiotics used in severe hospital-acquired infections, including those caused by Gram-negative pathogens.

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inventory 25mg
10-20 days ฿26,340.00

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(2S,5R)-6,6-Dibromo-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide
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Widely used in the pharmaceutical industry as an intermediate in the synthesis of carbapenem antibiotics. These antibiotics are known for their broad-spectrum activity and resistance to beta-lactamases, making them effective against multidrug-resistant bacterial infections. The compound's structure enables enhanced stability and reactivity in forming key beta-lactam ring systems essential for antimicrobial activity. It plays a critical role in producing potent antibiotics used in severe hospital-acquired

Widely used in the pharmaceutical industry as an intermediate in the synthesis of carbapenem antibiotics. These antibiotics are known for their broad-spectrum activity and resistance to beta-lactamases, making them effective against multidrug-resistant bacterial infections. The compound's structure enables enhanced stability and reactivity in forming key beta-lactam ring systems essential for antimicrobial activity. It plays a critical role in producing potent antibiotics used in severe hospital-acquired infections, including those caused by Gram-negative pathogens.

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