2-(3-carboxy-4-chlorophenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carboxylic acid

95%

Reagent Code: #163324
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CAS Number 524712-40-1

science Other reagents with same CAS 524712-40-1

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scatter_plot Molecular Information
Weight 311.63 g/mol
Formula C₁₁H₆ClN₃O₆
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antidiabetic agents. It plays a role in inhibiting specific enzymes involved in glucose metabolism, making it valuable in research for type 2 diabetes treatments. Also utilized in medicinal chemistry for structure-activity relationship studies due to its ability to interact with biological targets through hydrogen bonding and ionic interactions. Its functional groups allow for further chemical modifications, enabling the creation of derivative compounds with enhanced pharmacological properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,010.00
inventory 250mg
10-20 days ฿9,630.00

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2-(3-carboxy-4-chlorophenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carboxylic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antidiabetic agents. It plays a role in inhibiting specific enzymes involved in glucose metabolism, making it valuable in research for type 2 diabetes treatments. Also utilized in medicinal chemistry for structure-activity relationship studies due to its ability to interact with biological targets through hydrogen bonding and ionic interactions. Its functional groups allow for further chemical modific

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antidiabetic agents. It plays a role in inhibiting specific enzymes involved in glucose metabolism, making it valuable in research for type 2 diabetes treatments. Also utilized in medicinal chemistry for structure-activity relationship studies due to its ability to interact with biological targets through hydrogen bonding and ionic interactions. Its functional groups allow for further chemical modifications, enabling the creation of derivative compounds with enhanced pharmacological properties.

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