6-Amino-1,3-Dimethyl-2,4-Dioxo-1,2,3,4-Tetrahydropyrimidine-5-Carbaldehyde

≥95%

Reagent Code: #139228
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CAS Number 54660-80-9

science Other reagents with same CAS 54660-80-9

blur_circular Chemical Specifications

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Weight 183.17 g/mol
Formula C₇H₉N₃O₃
badge Registry Numbers
MDL Number MFCD00091834
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of pyrimidine-based drugs which exhibit antiviral, anticancer, and antimicrobial activities. It serves as a building block in the preparation of fused heterocyclic compounds, including barbiturate derivatives and other bioactive molecules. Its aldehyde and amino functional groups allow for versatile chemical modifications, enabling the formation of Schiff bases, hydrazones, and other derivatives important in medicinal chemistry research. Also employed in the design of dyes and functional materials due to its conjugated structure and reactivity.

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inventory 25mg
10-20 days ฿2,570.00

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6-Amino-1,3-Dimethyl-2,4-Dioxo-1,2,3,4-Tetrahydropyrimidine-5-Carbaldehyde
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of pyrimidine-based drugs which exhibit antiviral, anticancer, and antimicrobial activities. It serves as a building block in the preparation of fused heterocyclic compounds, including barbiturate derivatives and other bioactive molecules. Its aldehyde and amino functional groups allow for versatile chemical modifications, enabling the formation of Schiff bases, hydrazones, and other derivatives important in medi

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of pyrimidine-based drugs which exhibit antiviral, anticancer, and antimicrobial activities. It serves as a building block in the preparation of fused heterocyclic compounds, including barbiturate derivatives and other bioactive molecules. Its aldehyde and amino functional groups allow for versatile chemical modifications, enabling the formation of Schiff bases, hydrazones, and other derivatives important in medicinal chemistry research. Also employed in the design of dyes and functional materials due to its conjugated structure and reactivity.

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