tert -Butyl [Bis(4-methoxyphenyl)phosphinyloxy]carbamate

≥95%

Reagent Code: #77831
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CAS Number 619333-95-8

science Other reagents with same CAS 619333-95-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 393.38 g/mol
Formula C₁₉H₂₄NO₆P
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis as a reagent for the protection of amines. It is particularly effective in peptide synthesis, where it safeguards amino groups during the formation of peptide bonds, ensuring selective reactions without unwanted side interactions. Additionally, it is employed in the synthesis of complex organic molecules, where its protective group can be easily removed under mild conditions, allowing for the precise construction of molecular structures. Its application extends to the development of pharmaceuticals, where it aids in the creation of active compounds with specific functional groups intact.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity 94.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,570.00
inventory 1g
10-20 days ฿5,330.00
inventory 5g
10-20 days ฿17,980.00

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tert -Butyl [Bis(4-methoxyphenyl)phosphinyloxy]carbamate
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This chemical is primarily utilized in organic synthesis as a reagent for the protection of amines. It is particularly effective in peptide synthesis, where it safeguards amino groups during the formation of peptide bonds, ensuring selective reactions without unwanted side interactions. Additionally, it is employed in the synthesis of complex organic molecules, where its protective group can be easily removed under mild conditions, allowing for the precise construction of molecular structures. Its applic

This chemical is primarily utilized in organic synthesis as a reagent for the protection of amines. It is particularly effective in peptide synthesis, where it safeguards amino groups during the formation of peptide bonds, ensuring selective reactions without unwanted side interactions. Additionally, it is employed in the synthesis of complex organic molecules, where its protective group can be easily removed under mild conditions, allowing for the precise construction of molecular structures. Its application extends to the development of pharmaceuticals, where it aids in the creation of active compounds with specific functional groups intact.

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