N-Boc-3-Amino-4-iodopyridine

≥98.0%

Reagent Code: #113322
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CAS Number 154048-89-2

science Other reagents with same CAS 154048-89-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.13 g/mol
Formula C₁₀H₁₃IN₂O₂
badge Registry Numbers
MDL Number MFCD04973410
thermostat Physical Properties
Boiling Point 313.221°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. It is particularly valuable in the development of drugs targeting neurological disorders, cancer, and infectious diseases. The Boc protecting group allows for selective reactions, enabling the introduction of other functional groups or further modifications. Its iodine substituent makes it a versatile building block for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating complex molecular structures. This compound is also employed in the synthesis of heterocyclic compounds, which are widely used in medicinal chemistry for their diverse biological activities.

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Test Parameter Specification
Appearance Light yellow to yellow solid
Purity (%) 97.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿460.00
inventory 250mg
10-20 days ฿790.00
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N-Boc-3-Amino-4-iodopyridine
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Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. It is particularly valuable in the development of drugs targeting neurological disorders, cancer, and infectious diseases. The Boc protecting group allows for selective reactions, enabling the introduction of other functional groups or further modifications. Its iodine substituent makes it a versatile building block for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating complex molecular structures. This compound is also employed in the synthesis of heterocyclic compounds, which are widely used in medicinal chemistry for their diverse biological activities.
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