tert-Butyl (4-aminobut-2-en-1-yl)carbamate

≥95%

Reagent Code: #148371
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CAS Number 1807939-98-5

science Other reagents with same CAS 1807939-98-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.25 g/mol
Formula C₉H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD09752966
thermostat Physical Properties
Boiling Point 307.8±35.0°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 biologically active compounds such as pharmaceuticals and agrochemicals. Its structure contains an allylic amine and a Boc-protected amine, making it valuable for constructing complex molecules through selective reactions. Commonly employed in the synthesis of nitrogen-containing heterocycles and peptide mimetics. Also utilized in medicinal chemistry for the development of kinase inhibitors and other targeted therapies due to its ability to act as a building block in multi-step routes toward drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,190.00
inventory 250mg
10-20 days ฿12,380.00

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tert-Butyl (4-aminobut-2-en-1-yl)carbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of biologically active compounds such as pharmaceuticals and agrochemicals. Its structure contains an allylic amine and a Boc-protected amine, making it valuable for constructing complex molecules through selective reactions. Commonly employed in the synthesis of nitrogen-containing heterocycles and peptide mimetics. Also utilized in medicinal chemistry for the development of kinase inhibitors and other targeted therapies due to i
Used as an intermediate in organic synthesis, particularly in the preparation of biologically active compounds such as pharmaceuticals and agrochemicals. Its structure contains an allylic amine and a Boc-protected amine, making it valuable for constructing complex molecules through selective reactions. Commonly employed in the synthesis of nitrogen-containing heterocycles and peptide mimetics. Also utilized in medicinal chemistry for the development of kinase inhibitors and other targeted therapies due to its ability to act as a building block in multi-step routes toward drug candidates.
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