tert-Butyl(4-hydroxypyridin-2-yl)carbamate

98%

Reagent Code: #155190
fingerprint
CAS Number 937263-39-3

science Other reagents with same CAS 937263-39-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.23 g/mol
Formula C₁₀H₁₄N₂O₃
badge Registry Numbers
MDL Number MFCD23378741
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing heterocyclic systems. Commonly employed in research settings to prepare derivatives with potential antiviral, anticancer, or anti-inflammatory activity. Also utilized in the design of prodrugs due to the presence of the hydroxyl and carbamate groups, which can be modified for improved solubility or metabolic stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,290.00
inventory 250mg
10-20 days ฿19,600.00
inventory 500mg
10-20 days ฿31,670.00
inventory 1g
10-20 days ฿40,170.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl(4-hydroxypyridin-2-yl)carbamate
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing heterocyclic systems. Commonly employed in research settings to prepare derivatives with potential antiviral, anticancer, or anti-inflammatory activity. Also utilized in the design of prodrugs due to the presence of the hydroxyl and carbamate

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing heterocyclic systems. Commonly employed in research settings to prepare derivatives with potential antiviral, anticancer, or anti-inflammatory activity. Also utilized in the design of prodrugs due to the presence of the hydroxyl and carbamate groups, which can be modified for improved solubility or metabolic stability.

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...