5,7-Dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic Acid

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Reagent Code: #172825
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CAS Number 90349-23-8

science Other reagents with same CAS 90349-23-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.19 g/mol
Formula C₉H₉N₃O₂
badge Registry Numbers
MDL Number MFCD01051014
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for treating inflammatory diseases and certain cancers. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency. Also employed in research for optimizing drug candidates due to its favorable metabolic stability and ability to form hydrogen bonds. Commonly utilized in medicinal chemistry for scaffold modification to improve pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,300.00
inventory 1g
10-20 days ฿3,130.00
inventory 5g
10-20 days ฿7,900.00
inventory 10g
10-20 days ฿15,510.00

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5,7-Dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic Acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for treating inflammatory diseases and certain cancers. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency. Also employed in research for optimizing drug candidates due to its favorable metabolic stability and ability to form hydrogen bonds. Commonly utilized in medicinal chemistry for scaffold modification to improve pharmacokinetic properti

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for treating inflammatory diseases and certain cancers. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency. Also employed in research for optimizing drug candidates due to its favorable metabolic stability and ability to form hydrogen bonds. Commonly utilized in medicinal chemistry for scaffold modification to improve pharmacokinetic properties.

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