N-BOC-2-IODOANILINE

97%

Reagent Code: #218612
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CAS Number 161117-84-6

science Other reagents with same CAS 161117-84-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.14 g/mol
Formula C₁₁H₁₄INO₂
badge Registry Numbers
MDL Number MFCD07369726
thermostat Physical Properties
Boiling Point 85-95 °C/0.5 mmHg (lit.)
inventory_2 Storage & Handling
Density 1.277 g/mL at 25 °C (lit.)
Storage Room temperature, dry, sealed, inflatable

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in palladium-catalyzed coupling reactions such as Suzuki or Buchwald-Hartwig aminations. The N-BOC protecting group stabilizes the amine functionality during reactions, while the iodine atom serves as a reactive site for cross-coupling. Commonly employed in the development of bioactive molecules, including drug candidates targeting central nervous system disorders and anti-inflammatory agents. Also utilized in the preparation of functionalized aniline derivatives for agrochemicals and materials science.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿3,150.00
N-BOC-2-IODOANILINE
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Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in palladium-catalyzed coupling reactions such as Suzuki or Buchwald-Hartwig aminations. The N-BOC protecting group stabilizes the amine functionality during reactions, while the iodine atom serves as a reactive site for cross-coupling. Commonly employed in the development of bioactive molecules, including drug candidates targeting central nervous system disorders and anti-inflammatory agents. Also utilized in th

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in palladium-catalyzed coupling reactions such as Suzuki or Buchwald-Hartwig aminations. The N-BOC protecting group stabilizes the amine functionality during reactions, while the iodine atom serves as a reactive site for cross-coupling. Commonly employed in the development of bioactive molecules, including drug candidates targeting central nervous system disorders and anti-inflammatory agents. Also utilized in the preparation of functionalized aniline derivatives for agrochemicals and materials science.

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