tert-Butyl (4-iodobutyl)carbamate

98%

Reagent Code: #36944
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CAS Number 262278-40-0

science Other reagents with same CAS 262278-40-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.1500 g/mol
Formula C₉H₁₈INO₂
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MDL Number MFCD09951820
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Storage room temperature

description Product Description

This chemical is primarily used in organic synthesis as a versatile intermediate. It is often employed in the preparation of complex molecules, particularly in pharmaceutical research and development. The tert-butyl group provides stability and protection for the carbamate functionality during chemical reactions, while the iodo group serves as a reactive site for further functionalization, such as cross-coupling reactions. Its applications include the synthesis of biologically active compounds, where it acts as a building block for creating drug candidates or other targeted molecules. Additionally, it is utilized in peptide chemistry for the protection of amino groups, enabling controlled modifications in peptide synthesis.

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Test Parameter Specification
Appearance Off-White to Light Yellow Liquid or Semi-Solid or Solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,251.00

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tert-Butyl (4-iodobutyl)carbamate
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This chemical is primarily used in organic synthesis as a versatile intermediate. It is often employed in the preparation of complex molecules, particularly in pharmaceutical research and development. The tert-butyl group provides stability and protection for the carbamate functionality during chemical reactions, while the iodo group serves as a reactive site for further functionalization, such as cross-coupling reactions. Its applications include the synthesis of biologically active compounds, where it

This chemical is primarily used in organic synthesis as a versatile intermediate. It is often employed in the preparation of complex molecules, particularly in pharmaceutical research and development. The tert-butyl group provides stability and protection for the carbamate functionality during chemical reactions, while the iodo group serves as a reactive site for further functionalization, such as cross-coupling reactions. Its applications include the synthesis of biologically active compounds, where it acts as a building block for creating drug candidates or other targeted molecules. Additionally, it is utilized in peptide chemistry for the protection of amino groups, enabling controlled modifications in peptide synthesis.

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