tert-butyl (3-bromophenyl)carbamate

98%

Reagent Code: #242090
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CAS Number 25216-74-4

science Other reagents with same CAS 25216-74-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.1384 g/mol
Formula C₁₁H₁₄BrNO₂
badge Registry Numbers
MDL Number MFCD01006618
thermostat Physical Properties
Melting Point 86-89 °C(lit)
Boiling Point 279.6±23.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.398±0.06 g/cm3(Predicted)
Storage Room temperature, dry, sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protected aniline derivative, where the tert-butoxycarbonyl (Boc) group stabilizes the amine during reactions, allowing selective functionalization at other sites. The bromine substituent enables further transformations via cross-coupling reactions such as Suzuki or Heck couplings, making it valuable in constructing complex aromatic systems for drug discovery. Commonly employed in the development of bioactive molecules where controlled amine reactivity is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿430.00
inventory 25g
10-20 days ฿774.00
inventory 100g
10-20 days ฿4,660.00

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tert-butyl (3-bromophenyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protected aniline derivative, where the tert-butoxycarbonyl (Boc) group stabilizes the amine during reactions, allowing selective functionalization at other sites. The bromine substituent enables further transformations via cross-coupling reactions such as Suzuki or Heck couplings, making it valuable in constructing complex aromatic systems for drug discovery. Commonly employ

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protected aniline derivative, where the tert-butoxycarbonyl (Boc) group stabilizes the amine during reactions, allowing selective functionalization at other sites. The bromine substituent enables further transformations via cross-coupling reactions such as Suzuki or Heck couplings, making it valuable in constructing complex aromatic systems for drug discovery. Commonly employed in the development of bioactive molecules where controlled amine reactivity is required.

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