Ethyl 3-Chloropyridazine-4-carboxylate

≥95%

Reagent Code: #171856
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CAS Number 1445-54-1

science Other reagents with same CAS 1445-54-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.60 g/mol
Formula C₇H₇ClN₂O₂
badge Registry Numbers
MDL Number MFCD12828685
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of pyridazine-based bioactive compounds. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for creating analogs with potential antihypertensive, anti-inflammatory, or antimicrobial activity. Also employed in agrochemical research for designing novel pesticides and herbicides due to the pyridazine ring’s favorable electronic properties. Commonly utilized in cross-coupling reactions and nucleophilic substitutions to build complex heterocyclic systems in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,260.00
inventory 1g
10-20 days ฿28,490.00
inventory 5g
10-20 days ฿98,720.00

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Ethyl 3-Chloropyridazine-4-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of pyridazine-based bioactive compounds. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for creating analogs with potential antihypertensive, anti-inflammatory, or antimicrobial activity. Also employed in agrochemical research for designing novel pesticides and herbicides due to the pyridazine ring’s favorable electronic properties. Commonly utilized in cro
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of pyridazine-based bioactive compounds. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for creating analogs with potential antihypertensive, anti-inflammatory, or antimicrobial activity. Also employed in agrochemical research for designing novel pesticides and herbicides due to the pyridazine ring’s favorable electronic properties. Commonly utilized in cross-coupling reactions and nucleophilic substitutions to build complex heterocyclic systems in drug discovery programs.
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