2-Amino-3,5-diiodo-6-hydroxypyridine hydrochloride

Reagent Code: #42107
fingerprint
CAS Number 856965-98-5

science Other reagents with same CAS 856965-98-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 361.91 g/mol
Formula C₅H₄I₂N₂O
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. Its structure allows for selective iodination, making it valuable in the development of iodine-containing drugs, particularly those targeting thyroid disorders. Additionally, it is employed in the synthesis of radiopharmaceuticals for diagnostic imaging, leveraging its iodine atoms for radioisotope labeling. The compound’s hydroxyl and amino groups also facilitate its use in the creation of complex molecules for medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Amino-3,5-diiodo-6-hydroxypyridine hydrochloride
No image available

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. Its structure allows for selective iodination, making it valuable in the development of iodine-containing drugs, particularly those targeting thyroid disorders. Additionally, it is employed in the synthesis of radiopharmaceuticals for diagnostic imaging, leveraging its iodine atoms for radioisotope labeling. The compound’s hydroxyl and amino groups also facilitate its use in the c

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. Its structure allows for selective iodination, making it valuable in the development of iodine-containing drugs, particularly those targeting thyroid disorders. Additionally, it is employed in the synthesis of radiopharmaceuticals for diagnostic imaging, leveraging its iodine atoms for radioisotope labeling. The compound’s hydroxyl and amino groups also facilitate its use in the creation of complex molecules for medicinal chemistry research.

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...