tert-Butyl 4-aminobutyl(methyl)carbamate

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Reagent Code: #148418
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CAS Number 144222-23-1

science Other reagents with same CAS 144222-23-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.29 g/mol
Formula C₁₀H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD03001681
thermostat Physical Properties
Boiling Point 276.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its protected amine functionality allows for selective reactions in multi-step syntheses. Commonly employed in the development of peptide mimetics and kinase inhibitors due to its ability to introduce a methylaminoalkyl spacer with orthogonal protection. Also utilized in the synthesis of functionalized polymers and as a building block in combinatorial chemistry for drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿710.00
inventory 1g
10-20 days ฿2,680.00
inventory 5g
10-20 days ฿9,530.00
inventory 10g
10-20 days ฿17,390.00
inventory 25g
10-20 days ฿37,750.00

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tert-Butyl 4-aminobutyl(methyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its protected amine functionality allows for selective reactions in multi-step syntheses. Commonly employed in the development of peptide mimetics and kinase inhibitors due to its ability to introduce a methylaminoalkyl spacer with orthogonal protection. Also utilized in the synthesis of functionalized polymers and as a building block in combinatorial chemistry for drug discovery.

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its protected amine functionality allows for selective reactions in multi-step syntheses. Commonly employed in the development of peptide mimetics and kinase inhibitors due to its ability to introduce a methylaminoalkyl spacer with orthogonal protection. Also utilized in the synthesis of functionalized polymers and as a building block in combinatorial chemistry for drug discovery.

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