tert-Butyl 3-(hydroxymethyl)-2-isopropyl-4,5-dihydro-2H-pyrazolo[3,4-c]pyridine-6(7H)-carboxylate

95%

Reagent Code: #150474
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CAS Number 1823389-31-6

science Other reagents with same CAS 1823389-31-6

blur_circular Chemical Specifications

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Weight 295.38 g/mol
Formula C₁₅H₂₅N₃O₃
badge Registry Numbers
MDL Number MFCD28119023
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure allows for selective modification, making it valuable in optimizing drug potency and metabolic stability during medicinal chemistry research. Commonly employed in late-stage functionalization to introduce the pyrazolopyridine scaffold, which is known for favorable binding to biological targets and improved pharmacokinetic profiles.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿19,360.00
inventory 100mg
10-20 days ฿46,240.00

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tert-Butyl 3-(hydroxymethyl)-2-isopropyl-4,5-dihydro-2H-pyrazolo[3,4-c]pyridine-6(7H)-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure allows for selective modification, making it valuable in optimizing drug potency and metabolic stability during medicinal chemistry research. Commonly employed in late-stage functionalization to introduce the pyrazolopyridine scaffold, which is known for favorable binding to biological targets and improved pharmacokinetic profiles.
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure allows for selective modification, making it valuable in optimizing drug potency and metabolic stability during medicinal chemistry research. Commonly employed in late-stage functionalization to introduce the pyrazolopyridine scaffold, which is known for favorable binding to biological targets and improved pharmacokinetic profiles.
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