tert-Butyl (2-iodoethyl)carbamate

95%

Reagent Code: #149636
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CAS Number 122234-46-2

science Other reagents with same CAS 122234-46-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.1 g/mol
Formula C₇H₁₄INO₂
badge Registry Numbers
MDL Number MFCD09951818
thermostat Physical Properties
Boiling Point 281.3±23.0 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Storage −20°C, dry, avoid light

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of nitrogen-containing compounds such as pharmaceuticals and agrochemicals. Its reactivity allows for the introduction of the tert-butyloxycarbonyl (Boc) protected aminoethyl group, which is valuable in multi-step syntheses where protection of amine functionalities is required. The iodine atom serves as a good leaving group, enabling further transformations via nucleophilic substitution or cross-coupling reactions. Commonly employed in the development of active pharmaceutical ingredients (APIs) where controlled amine reactivity is needed.

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Test Parameter Specification
Appearance Yellow solid powder
Purity (%) 94.5-100%
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,100.00
inventory 250mg
10-20 days ฿2,600.00
inventory 1g
10-20 days ฿6,030.00
inventory 5g
10-20 days ฿19,570.00

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tert-Butyl (2-iodoethyl)carbamate
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Used as a key intermediate in organic synthesis, particularly in the preparation of nitrogen-containing compounds such as pharmaceuticals and agrochemicals. Its reactivity allows for the introduction of the tert-butyloxycarbonyl (Boc) protected aminoethyl group, which is valuable in multi-step syntheses where protection of amine functionalities is required. The iodine atom serves as a good leaving group, enabling further transformations via nucleophilic substitution or cross-coupling reactions. Commonly employed in the development of active pharmaceutical ingredients (APIs) where controlled amine reactivity is needed.
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