Methyl 7-aminoquinoline-3-carboxylate

95%

Reagent Code: #84135
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CAS Number 948302-98-5

science Other reagents with same CAS 948302-98-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.21 g/mol
Formula C₁₁H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD18260993
inventory_2 Storage & Handling
Storage Room temperature, away from light, dry, sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring both an amino group and a carboxylate ester, makes it a versatile intermediate in the synthesis of heterocyclic compounds. These heterocycles are often explored for their potential biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it serves as a precursor in the preparation of fluorescent dyes and markers, which are valuable in biochemical and medical research for imaging and diagnostic purposes. Its quinoline core is also of interest in the design of materials with optoelectronic applications, such as organic light-emitting diodes (OLEDs) and sensors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,340.00
inventory 250mg
10-20 days ฿16,992.00

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Methyl 7-aminoquinoline-3-carboxylate
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This compound is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring both an amino group and a carboxylate ester, makes it a versatile intermediate in the synthesis of heterocyclic compounds. These heterocycles are often explored for their potential biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it serves as a precursor in the preparation

This compound is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring both an amino group and a carboxylate ester, makes it a versatile intermediate in the synthesis of heterocyclic compounds. These heterocycles are often explored for their potential biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it serves as a precursor in the preparation of fluorescent dyes and markers, which are valuable in biochemical and medical research for imaging and diagnostic purposes. Its quinoline core is also of interest in the design of materials with optoelectronic applications, such as organic light-emitting diodes (OLEDs) and sensors.

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