2-Amino-5-iodo-4-methylnicotinonitrile

95%

Reagent Code: #138466
fingerprint
CAS Number 180995-02-2

science Other reagents with same CAS 180995-02-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.05 g/mol
Formula C₇H₆IN₃
badge Registry Numbers
MDL Number MFCD09030796
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of heterocyclic systems important in drug design. The iodo and amino functional groups allow for further derivatization through cross-coupling reactions and nucleophilic substitutions, making it valuable in medicinal chemistry for creating diverse compound libraries. Also employed in the preparation of agrochemicals and functional materials due to its reactive scaffold.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,970.00
inventory 250mg
10-20 days ฿8,450.00
inventory 1g
10-20 days ฿17,990.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Amino-5-iodo-4-methylnicotinonitrile
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of heterocyclic systems important in drug design. The iodo and amino functional groups allow for further derivatization through cross-coupling reactions and nucleophilic substitutions, making it valuable in medicinal chemistry for creating diverse compound libraries. Also employed in the preparation of agroche

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of heterocyclic systems important in drug design. The iodo and amino functional groups allow for further derivatization through cross-coupling reactions and nucleophilic substitutions, making it valuable in medicinal chemistry for creating diverse compound libraries. Also employed in the preparation of agrochemicals and functional materials due to its reactive scaffold.

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...