Acetic 2-(2,5-dioxopyrrolidin-1-yl)propanoic thioanhydride

98%

Reagent Code: #122013
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CAS Number 1093759-04-6

science Other reagents with same CAS 1093759-04-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.25 g/mol
Formula C₉H₁₁NO₄S
badge Registry Numbers
MDL Number MFCD11519182
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily utilized in the synthesis of various organic compounds, particularly in the field of peptide chemistry. It acts as a coupling agent, facilitating the formation of peptide bonds between amino acids during solid-phase peptide synthesis. Its thioanhydride group is reactive and enables efficient condensation reactions, making it valuable for producing peptides with high purity and yield. Additionally, it is employed in the preparation of functionalized polymers and materials, where its reactive properties allow for the incorporation of specific chemical groups into polymer chains. Its application extends to the development of drug delivery systems, where it can be used to create biodegradable and biocompatible polymers tailored for controlled release of therapeutic agents.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,016.00
1g
10-20 days ฿5,436.00
100mg
10-20 days ฿1,188.00
Acetic 2-(2,5-dioxopyrrolidin-1-yl)propanoic thioanhydride
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This chemical is primarily utilized in the synthesis of various organic compounds, particularly in the field of peptide chemistry. It acts as a coupling agent, facilitating the formation of peptide bonds between amino acids during solid-phase peptide synthesis. Its thioanhydride group is reactive and enables efficient condensation reactions, making it valuable for producing peptides with high purity and yield. Additionally, it is employed in the preparation of functionalized polymers and materials, where

This chemical is primarily utilized in the synthesis of various organic compounds, particularly in the field of peptide chemistry. It acts as a coupling agent, facilitating the formation of peptide bonds between amino acids during solid-phase peptide synthesis. Its thioanhydride group is reactive and enables efficient condensation reactions, making it valuable for producing peptides with high purity and yield. Additionally, it is employed in the preparation of functionalized polymers and materials, where its reactive properties allow for the incorporation of specific chemical groups into polymer chains. Its application extends to the development of drug delivery systems, where it can be used to create biodegradable and biocompatible polymers tailored for controlled release of therapeutic agents.

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