Tert-butyl (3-iodopropyl)carbamate

95%

Reagent Code: #242608
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CAS Number 167479-01-8

science Other reagents with same CAS 167479-01-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.12 g/mol
Formula C₈H₁₆INO₂
badge Registry Numbers
MDL Number MFCD09951819
thermostat Physical Properties
Boiling Point 299.3±23.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, inert gas storage

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its iodine functionality allows for further coupling reactions, such as Suzuki or Stille cross-couplings, enabling the construction of complex organic structures. The tert-butyl carbamate (Boc) group acts as a protected amine, which is stable under a variety of reaction conditions and can be easily deprotected to release the free amine when needed. This makes the compound valuable in multi-step synthesis, especially in medicinal chemistry for developing nitrogen-containing compounds like amines, amino acids, and heterocycles.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,580.00
inventory 250mg
10-20 days ฿2,700.00
inventory 1g
10-20 days ฿5,390.00

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Tert-butyl (3-iodopropyl)carbamate
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its iodine functionality allows for further coupling reactions, such as Suzuki or Stille cross-couplings, enabling the construction of complex organic structures. The tert-butyl carbamate (Boc) group acts as a protected amine, which is stable under a variety of reaction conditions and can be easily deprotected to release the free amine when needed. This makes the compound valuable

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its iodine functionality allows for further coupling reactions, such as Suzuki or Stille cross-couplings, enabling the construction of complex organic structures. The tert-butyl carbamate (Boc) group acts as a protected amine, which is stable under a variety of reaction conditions and can be easily deprotected to release the free amine when needed. This makes the compound valuable in multi-step synthesis, especially in medicinal chemistry for developing nitrogen-containing compounds like amines, amino acids, and heterocycles.

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