N-(8-Bromo-6-oxo-6,9-dihydro-1H-purin-2-yl)pivalamide

95%

Reagent Code: #219637
fingerprint
CAS Number 136675-83-7

science Other reagents with same CAS 136675-83-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.14 g/mol
Formula C₁₀H₁₂BrN₅O₂
badge Registry Numbers
MDL Number MFCD28142277
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of selective kinase inhibitors, particularly in the development of pharmaceuticals targeting inflammatory diseases and certain cancers. Its structure enables effective binding to specific enzyme active sites, enhancing drug potency. Commonly employed in medicinal chemistry for optimizing metabolic stability and bioavailability in adenosine receptor modulators. Also utilized in research settings to design analogs with improved selectivity and reduced off-target effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,400.00
inventory 250mg
10-20 days ฿4,800.00
inventory 1g
10-20 days ฿13,200.00
inventory 5g
10-20 days ฿49,990.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(8-Bromo-6-oxo-6,9-dihydro-1H-purin-2-yl)pivalamide
No image available

Used as a key intermediate in the synthesis of selective kinase inhibitors, particularly in the development of pharmaceuticals targeting inflammatory diseases and certain cancers. Its structure enables effective binding to specific enzyme active sites, enhancing drug potency. Commonly employed in medicinal chemistry for optimizing metabolic stability and bioavailability in adenosine receptor modulators. Also utilized in research settings to design analogs with improved selectivity and reduced off-target

Used as a key intermediate in the synthesis of selective kinase inhibitors, particularly in the development of pharmaceuticals targeting inflammatory diseases and certain cancers. Its structure enables effective binding to specific enzyme active sites, enhancing drug potency. Commonly employed in medicinal chemistry for optimizing metabolic stability and bioavailability in adenosine receptor modulators. Also utilized in research settings to design analogs with improved selectivity and reduced off-target effects.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...