1,8-Naphthyridine-2-carbaldehyde

95%

Reagent Code: #218743
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CAS Number 64379-45-9

science Other reagents with same CAS 64379-45-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.16 g/mol
Formula C₉H₆N₂O
badge Registry Numbers
MDL Number MFCD04971934
thermostat Physical Properties
Boiling Point 331.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, closed

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antibacterial and antiviral agents. Its structure serves as a key building block in heterocyclic chemistry, enabling the formation of complex nitrogen-containing compounds. Commonly employed in organic research for constructing fused ring systems and as a ligand in coordination chemistry for catalytic applications. Also utilized in the preparation of fluorescent probes due to its ability to form conjugated systems useful in sensing metal ions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,890.00
inventory 250mg
10-20 days ฿10,340.00
inventory 1g
10-20 days ฿28,390.00
1,8-Naphthyridine-2-carbaldehyde
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of antibacterial and antiviral agents. Its structure serves as a key building block in heterocyclic chemistry, enabling the formation of complex nitrogen-containing compounds. Commonly employed in organic research for constructing fused ring systems and as a ligand in coordination chemistry for catalytic applications. Also utilized in the preparation of fluorescent probes due to its ability to form conjugated systems u

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antibacterial and antiviral agents. Its structure serves as a key building block in heterocyclic chemistry, enabling the formation of complex nitrogen-containing compounds. Commonly employed in organic research for constructing fused ring systems and as a ligand in coordination chemistry for catalytic applications. Also utilized in the preparation of fluorescent probes due to its ability to form conjugated systems useful in sensing metal ions.

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