2-Chloro-3-iodopyridin-4-amine

97%

Reagent Code: #59154
fingerprint
CAS Number 909036-46-0

science Other reagents with same CAS 909036-46-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.46 g/mol
Formula C₅H₄ClIN₂
badge Registry Numbers
MDL Number MFCD09763660
thermostat Physical Properties
Melting Point 116-117°C
Boiling Point 377°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of organic synthesis as a versatile building block for the development of more complex chemical structures. It serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its unique structure, featuring both chloro and iodo substituents, allows for selective functionalization, making it valuable in cross-coupling reactions such as Suzuki or Sonogashira reactions. Additionally, it is employed in the preparation of agrochemicals, where it contributes to the development of compounds with potential pesticidal or herbicidal properties. Its role in medicinal chemistry also extends to the design of molecules for drug discovery, particularly in the optimization of drug candidates for improved efficacy and safety.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿486.00
inventory 1g
10-20 days ฿828.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Chloro-3-iodopyridin-4-amine
No image available
This compound is primarily utilized in the field of organic synthesis as a versatile building block for the development of more complex chemical structures. It serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its unique structure, featuring both chloro and iodo substituents, allows for selective functionalization, making it valuable in cross-coupling reactions such as Suzuki or Sonogashira reactions. Additionally, it is employed in the preparation of agrochemicals, where it contributes to the development of compounds with potential pesticidal or herbicidal properties. Its role in medicinal chemistry also extends to the design of molecules for drug discovery, particularly in the optimization of drug candidates for improved efficacy and safety.
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...