Tert-butyln-(2-aminoethyl)-n-cyclopropylcarbamate

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Reagent Code: #244498
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CAS Number 1247174-47-5

science Other reagents with same CAS 1247174-47-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.28 g/mol
Formula C₁₀H₂₀N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where a protected amine functionality is required. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactivity in multi-step syntheses. Its structure, featuring both cyclopropyl and aminoethyl components, makes it valuable in medicinal chemistry for constructing drug candidates targeting central nervous system disorders and metabolic diseases. Commonly employed in research settings for optimizing bioavailability and stability of amine-containing molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,020.00
inventory 1g
10-20 days ฿19,420.00
inventory 5g
10-20 days ฿60,880.00
inventory 250mg
10-20 days ฿6,980.00
inventory 500mg
10-20 days ฿13,210.00

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Tert-butyln-(2-aminoethyl)-n-cyclopropylcarbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where a protected amine functionality is required. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactivity in multi-step syntheses. Its structure, featuring both cyclopropyl and aminoethyl components, makes it valuable in medicinal chemistry for constructing drug candidates targeting central nervous system disorder

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where a protected amine functionality is required. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactivity in multi-step syntheses. Its structure, featuring both cyclopropyl and aminoethyl components, makes it valuable in medicinal chemistry for constructing drug candidates targeting central nervous system disorders and metabolic diseases. Commonly employed in research settings for optimizing bioavailability and stability of amine-containing molecules.

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