tert-Butyl (2-(benzylamino)ethyl)carbamate

≥95%

Reagent Code: #113077
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CAS Number 174799-52-1

science Other reagents with same CAS 174799-52-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.34 g/mol
Formula C₁₄H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD04114275
thermostat Physical Properties
Boiling Point 376.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is primarily utilized in organic synthesis as a protecting group for amines. Its structure allows it to shield amine functionalities during complex reactions, ensuring selectivity and preventing unwanted side reactions. It is particularly useful in peptide synthesis, where it protects amino groups while other segments of the molecule undergo chemical transformations. Additionally, it finds application in the development of pharmaceuticals, where it aids in the stepwise construction of drug molecules, ensuring precise control over the reaction process. Its stability under various conditions makes it a reliable choice in multi-step synthetic pathways.

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Test Parameter Specification
Appearance Yellow Viscous Liquid
Purity (%) 95-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,080.00
inventory 10g
10-20 days ฿9,405.00
inventory 5g
10-20 days ฿4,860.00

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tert-Butyl (2-(benzylamino)ethyl)carbamate
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This chemical is primarily utilized in organic synthesis as a protecting group for amines. Its structure allows it to shield amine functionalities during complex reactions, ensuring selectivity and preventing unwanted side reactions. It is particularly useful in peptide synthesis, where it protects amino groups while other segments of the molecule undergo chemical transformations. Additionally, it finds application in the development of pharmaceuticals, where it aids in the stepwise construction of drug

This chemical is primarily utilized in organic synthesis as a protecting group for amines. Its structure allows it to shield amine functionalities during complex reactions, ensuring selectivity and preventing unwanted side reactions. It is particularly useful in peptide synthesis, where it protects amino groups while other segments of the molecule undergo chemical transformations. Additionally, it finds application in the development of pharmaceuticals, where it aids in the stepwise construction of drug molecules, ensuring precise control over the reaction process. Its stability under various conditions makes it a reliable choice in multi-step synthetic pathways.

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