Ethyl 4-hydroxy-7-methyl-1,8-naphthyridine-3-carboxylate

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Reagent Code: #130731
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CAS Number 13250-96-9

science Other reagents with same CAS 13250-96-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.24 g/mol
Formula C₁₂H₁₂N₂O₃
badge Registry Numbers
MDL Number MFCD00234797
thermostat Physical Properties
Melting Point 272-273 °C
Boiling Point 350.5±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.296±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antibacterial and antiviral drugs. Its naphthyridine core structure contributes to binding with enzymes involved in nucleic acid synthesis, making it valuable in medicinal chemistry. Also employed in research for designing fluorescent probes due to its ability to exhibit photoluminescent properties under certain conditions. Commonly utilized in organic synthesis to build more complex heterocyclic systems for drug discovery and material science applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,600.00
inventory 250mg
10-20 days ฿4,390.00
inventory 1g
10-20 days ฿11,770.00

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Ethyl 4-hydroxy-7-methyl-1,8-naphthyridine-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antibacterial and antiviral drugs. Its naphthyridine core structure contributes to binding with enzymes involved in nucleic acid synthesis, making it valuable in medicinal chemistry. Also employed in research for designing fluorescent probes due to its ability to exhibit photoluminescent properties under certain conditions. Commonly utilized in organic synthesis to build more complex heterocyclic syst

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antibacterial and antiviral drugs. Its naphthyridine core structure contributes to binding with enzymes involved in nucleic acid synthesis, making it valuable in medicinal chemistry. Also employed in research for designing fluorescent probes due to its ability to exhibit photoluminescent properties under certain conditions. Commonly utilized in organic synthesis to build more complex heterocyclic systems for drug discovery and material science applications.

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