Pyrrolo[1,2-a]pyrimidine-8-carbonitrile, 4-hydroxy-2,7-dimethyl-

97%

Reagent Code: #223380
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CAS Number 2183215-98-5

science Other reagents with same CAS 2183215-98-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.198 g/mol
Formula C₁₀H₉N₃O
badge Registry Numbers
MDL Number MFCD32869259
inventory_2 Storage & Handling
Density 1.29±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting cancer-related enzymes. Its structure supports activity in modulating cell signaling pathways, making it valuable in the development of antitumor agents. Also explored in the design of anti-inflammatory and antiviral compounds due to its ability to interact with biological targets involved in disease progression. The hydroxy and nitrile functional groups enhance binding affinity and solubility, improving drug-like properties in candidate molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿22,080.00
1g
10-20 days ฿48,000.00
Pyrrolo[1,2-a]pyrimidine-8-carbonitrile, 4-hydroxy-2,7-dimethyl-
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting cancer-related enzymes. Its structure supports activity in modulating cell signaling pathways, making it valuable in the development of antitumor agents. Also explored in the design of anti-inflammatory and antiviral compounds due to its ability to interact with biological targets involved in disease progression. The hydroxy and nitrile functional groups enhance binding affinity and sol

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting cancer-related enzymes. Its structure supports activity in modulating cell signaling pathways, making it valuable in the development of antitumor agents. Also explored in the design of anti-inflammatory and antiviral compounds due to its ability to interact with biological targets involved in disease progression. The hydroxy and nitrile functional groups enhance binding affinity and solubility, improving drug-like properties in candidate molecules.

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