Dipyrrolidino(N-succinimidyloxy)carbenium hexafluorophosphate

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Reagent Code: #56703
label
Alias Dipyrrolidinyl(N-succinimidyloxy)carbenium hexafluorophosphate
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CAS Number 207683-26-9

science Other reagents with same CAS 207683-26-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 411.28 g/mol
Formula C₁₃H₂₀F₆N₃O₃P
badge Registry Numbers
MDL Number MFCD00192457
thermostat Physical Properties
Melting Point 152-154 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a coupling reagent in peptide synthesis, facilitating the formation of amide bonds between amino acids. It is particularly effective in solid-phase peptide synthesis, ensuring high yields and minimal racemization. Additionally, it is employed in the preparation of complex organic molecules, where it aids in the activation of carboxylic acids for subsequent reactions. Its stability and reactivity make it a valuable tool in medicinal chemistry for the development of pharmaceutical compounds.

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Test Parameter Specification
Melting point 152-154
Purity (HPLC) 98-100
Appearance White powder crystals

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,080.00
inventory 5g
10-20 days ฿3,010.00
inventory 25g
10-20 days ฿13,500.00

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Dipyrrolidino(N-succinimidyloxy)carbenium hexafluorophosphate
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Used as a coupling reagent in peptide synthesis, facilitating the formation of amide bonds between amino acids. It is particularly effective in solid-phase peptide synthesis, ensuring high yields and minimal racemization. Additionally, it is employed in the preparation of complex organic molecules, where it aids in the activation of carboxylic acids for subsequent reactions. Its stability and reactivity make it a valuable tool in medicinal chemistry for the development of pharmaceutical compounds.

Used as a coupling reagent in peptide synthesis, facilitating the formation of amide bonds between amino acids. It is particularly effective in solid-phase peptide synthesis, ensuring high yields and minimal racemization. Additionally, it is employed in the preparation of complex organic molecules, where it aids in the activation of carboxylic acids for subsequent reactions. Its stability and reactivity make it a valuable tool in medicinal chemistry for the development of pharmaceutical compounds.

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