(4R,12aS)-7-Methoxy-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1’,2’:4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxylic Acid

95%

Reagent Code: #36961
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CAS Number 1335210-34-8

science Other reagents with same CAS 1335210-34-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.29 g/mol
Formula C₁₄H₁₆N₂O₆
badge Registry Numbers
MDL Number MFCD28978321
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of more complex molecules, particularly those with therapeutic potential. Its structure is often leveraged in the development of antibiotics and antiviral agents, where its unique heterocyclic framework contributes to biological activity. Researchers explore its role in inhibiting specific enzymes or proteins involved in microbial or viral replication, making it valuable in drug discovery. Additionally, its methoxy and carboxylic acid functional groups provide sites for further chemical modifications, enabling the creation of derivatives with enhanced efficacy or reduced side effects. Its application is particularly prominent in the design of novel treatments for infectious diseases.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 94.5-100
NMR Conforms to Structure

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inventory 1g
10-20 days ฿97,470.00

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(4R,12aS)-7-Methoxy-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1’,2’:4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxylic Acid
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This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of more complex molecules, particularly those with therapeutic potential. Its structure is often leveraged in the development of antibiotics and antiviral agents, where its unique heterocyclic framework contributes to biological activity. Researchers explore its role in inhibiting specific enzymes or proteins involved in microbial or viral replication, making it valuable in drug discovery. Additionally, its methoxy and carboxylic acid functional groups provide sites for further chemical modifications, enabling the creation of derivatives with enhanced efficacy or reduced side effects. Its application is particularly prominent in the design of novel treatments for infectious diseases.
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