2-aminopyrimidine-4-carboxylic acid

95%

Reagent Code: #135109
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CAS Number 2164-65-0

science Other reagents with same CAS 2164-65-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.11 g/mol
Formula C₅H₅N₃O₂
badge Registry Numbers
MDL Number MFCD07783936
thermostat Physical Properties
Melting Point 285 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure serves as a building block for pyrimidine-based drugs, which can interfere with nucleic acid synthesis in pathogens or tumor cells. Also employed in the preparation of agrochemicals and functional materials due to its ability to form stable heterocyclic compounds. Its amino and carboxylic functional groups allow for easy modification, enabling the creation of diverse derivatives for drug discovery and material science applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿700.00
inventory 250mg
10-20 days ฿1,510.00
inventory 1g
10-20 days ฿4,950.00

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2-aminopyrimidine-4-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure serves as a building block for pyrimidine-based drugs, which can interfere with nucleic acid synthesis in pathogens or tumor cells. Also employed in the preparation of agrochemicals and functional materials due to its ability to form stable heterocyclic compounds. Its amino and carboxylic functional groups allow for easy modification, enabling the creation of d

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure serves as a building block for pyrimidine-based drugs, which can interfere with nucleic acid synthesis in pathogens or tumor cells. Also employed in the preparation of agrochemicals and functional materials due to its ability to form stable heterocyclic compounds. Its amino and carboxylic functional groups allow for easy modification, enabling the creation of diverse derivatives for drug discovery and material science applications.

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