N-[2-(Trimethylsilyl)ethoxycarbonyloxy]succinimide

≥98%

Reagent Code: #60100
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CAS Number 78269-85-9

science Other reagents with same CAS 78269-85-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.33 g/mol
Formula C₁₀H₁₇NO₅Si
badge Registry Numbers
MDL Number MFCD02683467
thermostat Physical Properties
Melting Point 98-102°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used as a protecting reagent in organic synthesis, particularly for protecting amino groups during peptide synthesis. It is highly effective in forming stable carbamate derivatives with amino acids, which can be easily deprotected under mild conditions using fluoride ions (e.g., TBAF). Its application is crucial in the synthesis of complex peptides and proteins, where selective protection and deprotection of functional groups are required. Additionally, it is utilized in the development of pharmaceuticals and bioactive compounds, ensuring the integrity of amino groups during multi-step reactions. Its compatibility with various solvents and stability under different reaction conditions make it a versatile tool in synthetic chemistry.

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Test Parameter Specification
Appearance White to Off-White to Pale Yellow Powder or Crystals or Powder with Chunk(s) or Crystals with Chunk(s)
Purity (HPLC)(%) 98-100
Melting Point (℃) 98.0-102.0
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿369.00
inventory 1g
10-20 days ฿774.00

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N-[2-(Trimethylsilyl)ethoxycarbonyloxy]succinimide
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This chemical is primarily used as a protecting reagent in organic synthesis, particularly for protecting amino groups during peptide synthesis. It is highly effective in forming stable carbamate derivatives with amino acids, which can be easily deprotected under mild conditions using fluoride ions (e.g., TBAF). Its application is crucial in the synthesis of complex peptides and proteins, where selective protection and deprotection of functional groups are required. Additionally, it is utilized in the de

This chemical is primarily used as a protecting reagent in organic synthesis, particularly for protecting amino groups during peptide synthesis. It is highly effective in forming stable carbamate derivatives with amino acids, which can be easily deprotected under mild conditions using fluoride ions (e.g., TBAF). Its application is crucial in the synthesis of complex peptides and proteins, where selective protection and deprotection of functional groups are required. Additionally, it is utilized in the development of pharmaceuticals and bioactive compounds, ensuring the integrity of amino groups during multi-step reactions. Its compatibility with various solvents and stability under different reaction conditions make it a versatile tool in synthetic chemistry.

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