Potassium Bis(Boc)amide

≥95%

Reagent Code: #69696
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CAS Number 89004-82-0

science Other reagents with same CAS 89004-82-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.35 g/mol
Formula C₁₀H₁₈NO₄K
badge Registry Numbers
MDL Number MFCD28014567
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Potassium Bis(Boc)amide is widely used in organic synthesis as a versatile reagent, particularly in the protection of amines. Its primary application lies in the introduction of the Boc (tert-butoxycarbonyl) protecting group to amine functionalities, which is crucial in peptide synthesis and other multi-step organic reactions. The Boc group protects amines from unwanted reactions during complex synthetic processes, allowing for selective deprotection later without disrupting other functional groups. This reagent is especially valuable in pharmaceutical research and development, where precise control over molecular structures is essential. Additionally, it is employed in the synthesis of complex natural products and bioactive molecules, ensuring high yields and purity in the final products. Its stability and ease of use make it a preferred choice in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,736.00
inventory 1g
10-20 days ฿6,390.00

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Potassium Bis(Boc)amide
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Potassium Bis(Boc)amide is widely used in organic synthesis as a versatile reagent, particularly in the protection of amines. Its primary application lies in the introduction of the Boc (tert-butoxycarbonyl) protecting group to amine functionalities, which is crucial in peptide synthesis and other multi-step organic reactions. The Boc group protects amines from unwanted reactions during complex synthetic processes, allowing for selective deprotection later without disrupting other functional groups. This

Potassium Bis(Boc)amide is widely used in organic synthesis as a versatile reagent, particularly in the protection of amines. Its primary application lies in the introduction of the Boc (tert-butoxycarbonyl) protecting group to amine functionalities, which is crucial in peptide synthesis and other multi-step organic reactions. The Boc group protects amines from unwanted reactions during complex synthetic processes, allowing for selective deprotection later without disrupting other functional groups. This reagent is especially valuable in pharmaceutical research and development, where precise control over molecular structures is essential. Additionally, it is employed in the synthesis of complex natural products and bioactive molecules, ensuring high yields and purity in the final products. Its stability and ease of use make it a preferred choice in modern synthetic chemistry.

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