4-Chloro-5,5,7-trimethyl-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one

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Reagent Code: #156714
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CAS Number 2007917-52-2

science Other reagents with same CAS 2007917-52-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.65 g/mol
Formula C₉H₁₀ClN₃O
badge Registry Numbers
MDL Number MFCD29918556
thermostat Physical Properties
Boiling Point 428.1±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.299±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of anticancer agents. Its structure allows selective binding to ATP sites in protein kinases, making it valuable in targeted therapies for tumors. Commonly employed in medicinal chemistry for optimizing potency and selectivity in drug candidates. Also utilized in the preparation of small-molecule inhibitors for inflammatory and neurodegenerative diseases due to its favorable pharmacokinetic profile.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,430.00
inventory 500mg
10-20 days ฿3,230.00

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4-Chloro-5,5,7-trimethyl-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one
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Used as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of anticancer agents. Its structure allows selective binding to ATP sites in protein kinases, making it valuable in targeted therapies for tumors. Commonly employed in medicinal chemistry for optimizing potency and selectivity in drug candidates. Also utilized in the preparation of small-molecule inhibitors for inflammatory and neurodegenerative diseases due to its favorable pharmacokinetic profile.

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of anticancer agents. Its structure allows selective binding to ATP sites in protein kinases, making it valuable in targeted therapies for tumors. Commonly employed in medicinal chemistry for optimizing potency and selectivity in drug candidates. Also utilized in the preparation of small-molecule inhibitors for inflammatory and neurodegenerative diseases due to its favorable pharmacokinetic profile.

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