tert-butyl N-[1,3-bis(phenylmethoxy)propan-2-yl]carbamate

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Reagent Code: #82810
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CAS Number 167486-39-7

science Other reagents with same CAS 167486-39-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 371.47 g/mol
Formula C₂₂H₂₉NO₄
badge Registry Numbers
MDL Number MFCD29917053
thermostat Physical Properties
Boiling Point 505.6±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.091±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the preparation of complex molecules. It serves as a protecting group for amines during multi-step chemical reactions, ensuring that the amine functionality remains intact while other parts of the molecule undergo transformations. This is especially useful in the synthesis of pharmaceuticals and biologically active compounds, where selective protection and deprotection of functional groups are crucial. Additionally, its structure, featuring tert-butyl and benzyl groups, makes it stable under various reaction conditions, allowing for its use in a wide range of synthetic processes. Its application is also seen in peptide synthesis, where it helps in the controlled assembly of amino acids into peptides without unwanted side reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿35,100.00
inventory 100mg
10-20 days ฿9,360.00
inventory 250mg
10-20 days ฿17,550.00

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tert-butyl N-[1,3-bis(phenylmethoxy)propan-2-yl]carbamate
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This chemical is primarily utilized in organic synthesis, particularly in the preparation of complex molecules. It serves as a protecting group for amines during multi-step chemical reactions, ensuring that the amine functionality remains intact while other parts of the molecule undergo transformations. This is especially useful in the synthesis of pharmaceuticals and biologically active compounds, where selective protection and deprotection of functional groups are crucial. Additionally, its structure,

This chemical is primarily utilized in organic synthesis, particularly in the preparation of complex molecules. It serves as a protecting group for amines during multi-step chemical reactions, ensuring that the amine functionality remains intact while other parts of the molecule undergo transformations. This is especially useful in the synthesis of pharmaceuticals and biologically active compounds, where selective protection and deprotection of functional groups are crucial. Additionally, its structure, featuring tert-butyl and benzyl groups, makes it stable under various reaction conditions, allowing for its use in a wide range of synthetic processes. Its application is also seen in peptide synthesis, where it helps in the controlled assembly of amino acids into peptides without unwanted side reactions.

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