(4-Iodo-pyridin-2-yl)-carbamic acid tert-butyl ester

98%

Reagent Code: #129308
fingerprint
CAS Number 405939-28-8

science Other reagents with same CAS 405939-28-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.13 g/mol
Formula C₁₀H₁₃IN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig aminations, to introduce the pyridine moiety into target molecules. Also utilized in the preparation of labeled compounds for medicinal chemistry research, including radiolabeled or fluorescent probes for biological studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,360.00
inventory 250mg
10-20 days ฿14,840.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4-Iodo-pyridin-2-yl)-carbamic acid tert-butyl ester
No image available

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig aminations, to introduce the pyridine moiety into target molecules. Also utilized in the preparation of labeled compounds for medicinal chemistry research, including rad

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig aminations, to introduce the pyridine moiety into target molecules. Also utilized in the preparation of labeled compounds for medicinal chemistry research, including radiolabeled or fluorescent probes for biological studies.

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...