Ethyl 2-methyl-3-oxo-1,2,3,4-tetrahydroquinoxaline-6-carboxylate

95%

Reagent Code: #184973
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CAS Number 1375900-45-0

science Other reagents with same CAS 1375900-45-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.25 g/mol
Formula C₁₂H₁₄N₂O₃
badge Registry Numbers
MDL Number MFCD22056396
inventory_2 Storage & Handling
Storage Room temperature, sealed, light-proof

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of heterocyclic frameworks common in medicinal chemistry. It is also employed in research settings for the preparation of fluorescent dyes and optoelectronic materials due to its conjugated system and ability to undergo functionalization. Commonly utilized in combinatorial chemistry and drug discovery for building complex quinoxaline-based scaffolds with potential anti-inflammatory, antiviral, or anticancer activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,960.00
inventory 250mg
10-20 days ฿11,830.00
inventory 1g
10-20 days ฿38,630.00

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Ethyl 2-methyl-3-oxo-1,2,3,4-tetrahydroquinoxaline-6-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of heterocyclic frameworks common in medicinal chemistry. It is also employed in research settings for the preparation of fluorescent dyes and optoelectronic materials due to its conjugated system and ability to undergo functionalization. Commonly utilized in combinatorial chemistry and drug discovery for building co

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of heterocyclic frameworks common in medicinal chemistry. It is also employed in research settings for the preparation of fluorescent dyes and optoelectronic materials due to its conjugated system and ability to undergo functionalization. Commonly utilized in combinatorial chemistry and drug discovery for building complex quinoxaline-based scaffolds with potential anti-inflammatory, antiviral, or anticancer activity.

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