2-Amino-5-iodo-3-methylpyridine

95%

Reagent Code: #135557
fingerprint
CAS Number 166266-19-9

science Other reagents with same CAS 166266-19-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.0400 g/mol
Formula C₆H₇IN₂
badge Registry Numbers
MDL Number MFCD02102422
thermostat Physical Properties
Melting Point 110.2-110.5℃
Boiling Point 303.4℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.898 g/cm3
Storage 2-8℃, dry

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, featuring amino and iodo groups, allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in research settings for designing compounds with potential anticancer, antiviral, or anti-inflammatory properties. Also utilized in the preparation of labeled compounds for metabolic studies due to the presence of iodine, which facilitates detection and imaging. The iodo substituent enables efficient copper- or palladium-catalyzed cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿470.00
inventory 5g
10-20 days ฿1,680.00
inventory 25g
10-20 days ฿5,940.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Amino-5-iodo-3-methylpyridine
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, featuring amino and iodo groups, allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in research settings for designing compounds with potential anticancer, antiviral, or anti-inflammatory properties. Also utilized in the preparation of labeled comp

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure, featuring amino and iodo groups, allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in research settings for designing compounds with potential anticancer, antiviral, or anti-inflammatory properties. Also utilized in the preparation of labeled compounds for metabolic studies due to the presence of iodine, which facilitates detection and imaging. The iodo substituent enables efficient copper- or palladium-catalyzed cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds.

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...