6-Chloro-1-methyluracil

95%

Reagent Code: #162399
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CAS Number 31737-09-4

science Other reagents with same CAS 31737-09-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.5584 g/mol
Formula C₅H₅ClN₂O₂
badge Registry Numbers
MDL Number MFCD09753498
thermostat Physical Properties
Melting Point 186 °C
inventory_2 Storage & Handling
Storage -20°C, inert gas, dry, sealed

description Product Description

Used in the synthesis of antiviral and anticancer agents, particularly as an intermediate in the preparation of pyrimidine-based nucleoside analogs. It serves as a building block in medicinal chemistry for developing compounds that interfere with viral replication or tumor cell proliferation. Also employed in research for modifying nucleic acid components to study structure-activity relationships. Its chloro and methyl functional groups allow selective substitutions, making it valuable in creating diverse derivatives for drug discovery.

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Test Parameter Specification
Appearance White solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,860.00
inventory 1g
10-20 days ฿6,011.50

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6-Chloro-1-methyluracil
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Used in the synthesis of antiviral and anticancer agents, particularly as an intermediate in the preparation of pyrimidine-based nucleoside analogs. It serves as a building block in medicinal chemistry for developing compounds that interfere with viral replication or tumor cell proliferation. Also employed in research for modifying nucleic acid components to study structure-activity relationships. Its chloro and methyl functional groups allow selective substitutions, making it valuable in creating divers

Used in the synthesis of antiviral and anticancer agents, particularly as an intermediate in the preparation of pyrimidine-based nucleoside analogs. It serves as a building block in medicinal chemistry for developing compounds that interfere with viral replication or tumor cell proliferation. Also employed in research for modifying nucleic acid components to study structure-activity relationships. Its chloro and methyl functional groups allow selective substitutions, making it valuable in creating diverse derivatives for drug discovery.

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