Ethyl 3-Oxo-3,4-dihydro-2-quinoxalinecarboxylate

≥97%

Reagent Code: #171833
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CAS Number 36818-07-2

science Other reagents with same CAS 36818-07-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.21 g/mol
Formula C₁₁H₁₀N₂O₃
badge Registry Numbers
MDL Number MFCD00459589
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anticoagulant and antithrombotic agents. It serves as a building block for heterocyclic compounds due to its reactive carbonyl and ester functional groups, enabling ring transformations and condensation reactions. Commonly employed in medicinal chemistry for constructing quinoxaline-based scaffolds, which exhibit biological activities such as kinase inhibition and antimicrobial effects. Also utilized in agrochemical research for designing bioactive molecules with potential pesticidal or herbicidal properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,600.00
inventory 5g
10-20 days ฿6,460.00
inventory 10g
10-20 days ฿7,880.00
inventory 25g
10-20 days ฿9,740.00

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Ethyl 3-Oxo-3,4-dihydro-2-quinoxalinecarboxylate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anticoagulant and antithrombotic agents. It serves as a building block for heterocyclic compounds due to its reactive carbonyl and ester functional groups, enabling ring transformations and condensation reactions. Commonly employed in medicinal chemistry for constructing quinoxaline-based scaffolds, which exhibit biological activities such as kinase inhibition and antimicrobial effects. Also utilized in agroch

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anticoagulant and antithrombotic agents. It serves as a building block for heterocyclic compounds due to its reactive carbonyl and ester functional groups, enabling ring transformations and condensation reactions. Commonly employed in medicinal chemistry for constructing quinoxaline-based scaffolds, which exhibit biological activities such as kinase inhibition and antimicrobial effects. Also utilized in agrochemical research for designing bioactive molecules with potential pesticidal or herbicidal properties.

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