6,7-Dihydro-1H-pyrrolo[3,4-d]pyrimidine-2,4(3H,5H)-dione hydrochloride

95%

Reagent Code: #178412
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CAS Number 13931-24-3

science Other reagents with same CAS 13931-24-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.6 g/mol
Formula C₆H₇N₃O₂.ClH
badge Registry Numbers
MDL Number MFCD11616742
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. It serves as a scaffold in the development of antiviral and anticancer agents due to its structural similarity to purine nucleosides. Its derivatives are explored for their potential in modulating cellular signaling pathways, especially in targeted cancer therapies. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,160.00
inventory 250mg
10-20 days ฿16,740.00
inventory 1g
10-20 days ฿44,370.00

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6,7-Dihydro-1H-pyrrolo[3,4-d]pyrimidine-2,4(3H,5H)-dione hydrochloride
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Used primarily in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. It serves as a scaffold in the development of antiviral and anticancer agents due to its structural similarity to purine nucleosides. Its derivatives are explored for their potential in modulating cellular signaling pathways, especially in targeted cancer therapies. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies to optim

Used primarily in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. It serves as a scaffold in the development of antiviral and anticancer agents due to its structural similarity to purine nucleosides. Its derivatives are explored for their potential in modulating cellular signaling pathways, especially in targeted cancer therapies. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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