2-Amino-4-iodopyrimidine

97%

Reagent Code: #135752
fingerprint
CAS Number 815610-16-3

science Other reagents with same CAS 815610-16-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221 g/mol
Formula C₄H₄IN₃
thermostat Physical Properties
Boiling Point 364.9°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the construction of nucleoside analogs, which can interfere with viral replication or tumor growth. Also employed in the preparation of functionalized pyrimidine derivatives for research in medicinal chemistry and drug discovery. The iodine substituent allows for further modification via cross-coupling reactions, making it valuable in building complex molecules for biological evaluation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿700.00
inventory 250mg
10-20 days ฿870.00
inventory 1g
10-20 days ฿2,920.00
inventory 5g
10-20 days ฿14,540.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Amino-4-iodopyrimidine
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the construction of nucleoside analogs, which can interfere with viral replication or tumor growth. Also employed in the preparation of functionalized pyrimidine derivatives for research in medicinal chemistry and drug discovery. The iodine substituent allows for further modification via cross-coupling reactions, making it valuable in building complex

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the construction of nucleoside analogs, which can interfere with viral replication or tumor growth. Also employed in the preparation of functionalized pyrimidine derivatives for research in medicinal chemistry and drug discovery. The iodine substituent allows for further modification via cross-coupling reactions, making it valuable in building complex molecules for biological evaluation.

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...