Ethyl 1-formyl-4-oxo-4H-quinolizine-3-carboxylate
≥95%
Reagent
Code: #114883
CAS Number
337909-10-1
blur_circular Chemical Specifications
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Molecular Information
Weight
245.23 g/mol
Formula
C₁₃H₁₁NO₄
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Registry Numbers
MDL Number
MFCD11111264
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Physical Properties
Boiling Point
446.8±45.0°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, store under inert gas
description Product Description
This chemical is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex heterocyclic compounds. Its unique structure, featuring both formyl and carboxylate functional groups, makes it a versatile building block in the synthesis of quinolizine derivatives, which are of significant interest in medicinal chemistry. Researchers often employ it to create potential drug candidates, particularly for targeting various biological pathways. Additionally, it has been explored in the design of novel fluorescent dyes and sensors due to its conjugated system, which can exhibit interesting photophysical properties. Its application extends to agrochemical research, where it serves as a precursor for developing compounds with potential pesticidal or herbicidal activities.
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Ethyl 1-formyl-4-oxo-4H-quinolizine-3-carboxylate
This chemical is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex heterocyclic compounds. Its unique structure, featuring both formyl and carboxylate functional groups, makes it a versatile building block in the synthesis of quinolizine derivatives, which are of significant interest in medicinal chemistry. Researchers often employ it to create potential drug candidates, particularly for targeting various biological pathways. Additionally, it has been explored in the design of novel fluorescent dyes and sensors due to its conjugated system, which can exhibit interesting photophysical properties. Its application extends to agrochemical research, where it serves as a precursor for developing compounds with potential pesticidal or herbicidal activities.
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