2-Bromo-N-(2-bromoethyl)-N-Cbz-ethanamine

96%

Reagent Code: #154543
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CAS Number 189323-09-9

science Other reagents with same CAS 189323-09-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 365.065 g/mol
Formula C₁₂H₁₅Br₂NO₂
thermostat Physical Properties
Boiling Point 402.3±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.619±0.06 g/cm3(Predicted)
Storage -20°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of complex organic molecules, particularly in pharmaceuticals and bioactive compounds. Its functional groups allow for selective reactions, making it valuable in constructing nitrogen-containing heterocycles and amine derivatives. Commonly employed in the preparation of protected aminoalkyl building blocks for peptide-like structures. The bromo groups enable alkylation and cross-coupling reactions, useful in medicinal chemistry for developing drug candidates. Also applied in the design of ligands and functionalized polymers due to its bifunctional reactivity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,610.00
inventory 5g
10-20 days ฿25,820.00

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2-Bromo-N-(2-bromoethyl)-N-Cbz-ethanamine
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Used as an intermediate in the synthesis of complex organic molecules, particularly in pharmaceuticals and bioactive compounds. Its functional groups allow for selective reactions, making it valuable in constructing nitrogen-containing heterocycles and amine derivatives. Commonly employed in the preparation of protected aminoalkyl building blocks for peptide-like structures. The bromo groups enable alkylation and cross-coupling reactions, useful in medicinal chemistry for developing drug candidates. Also

Used as an intermediate in the synthesis of complex organic molecules, particularly in pharmaceuticals and bioactive compounds. Its functional groups allow for selective reactions, making it valuable in constructing nitrogen-containing heterocycles and amine derivatives. Commonly employed in the preparation of protected aminoalkyl building blocks for peptide-like structures. The bromo groups enable alkylation and cross-coupling reactions, useful in medicinal chemistry for developing drug candidates. Also applied in the design of ligands and functionalized polymers due to its bifunctional reactivity.

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