N,N-DiBoc-2-amino-4-bromopyridine

95%

Reagent Code: #217329
fingerprint
CAS Number 1216620-65-3

science Other reagents with same CAS 1216620-65-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.24 g/mol
Formula C₁₅H₂₁BrN₂O₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a protected intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyridine-based active ingredients. The Boc (tert-butoxycarbonyl) groups provide amine protection during multi-step reactions, allowing selective functionalization at other sites of the molecule. The bromine substituent enables further coupling reactions, such as palladium-catalyzed cross-couplings (e.g., Suzuki or Buchwald-Hartwig), making it valuable in building complex heterocyclic systems. Commonly employed in medicinal chemistry for constructing kinase inhibitors and other bioactive molecules where the pyridine scaffold is essential.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿980.00
inventory 250mg
10-20 days ฿2,840.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N,N-DiBoc-2-amino-4-bromopyridine
No image available

Used as a protected intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyridine-based active ingredients. The Boc (tert-butoxycarbonyl) groups provide amine protection during multi-step reactions, allowing selective functionalization at other sites of the molecule. The bromine substituent enables further coupling reactions, such as palladium-catalyzed cross-couplings (e.g., Suzuki or Buchwald-Hartwig), making it valuable in building complex heterocyclic

Used as a protected intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyridine-based active ingredients. The Boc (tert-butoxycarbonyl) groups provide amine protection during multi-step reactions, allowing selective functionalization at other sites of the molecule. The bromine substituent enables further coupling reactions, such as palladium-catalyzed cross-couplings (e.g., Suzuki or Buchwald-Hartwig), making it valuable in building complex heterocyclic systems. Commonly employed in medicinal chemistry for constructing kinase inhibitors and other bioactive molecules where the pyridine scaffold is essential.

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...