1-((2-(Trimethylsilyl)Ethoxy)Methyl)-1H-1,2,4-Triazole

95%

  • Product Code: 88134
  CAS:    136118-56-4
Molecular Weight: 199.33 g./mol Molecular Formula: C₈H₁₇N₃OSi
EC Number: MDL Number: MFCD27997533
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily used in organic synthesis as a protecting group for alcohols and other functional groups. Its trimethylsilyl ethoxymethyl (SEM) group is effective in shielding reactive sites during complex chemical reactions, particularly in the synthesis of pharmaceuticals and fine chemicals. The SEM group is stable under various reaction conditions but can be selectively removed under mild acidic conditions, making it a versatile tool in multi-step synthetic processes. Additionally, it finds application in the preparation of heterocyclic compounds, where it aids in controlling the reactivity and selectivity of intermediates. Its utility in peptide synthesis and the development of bioactive molecules further highlights its importance in medicinal chemistry.
Product Specification:
Test Specification
APPEARANCE Colorless to light yellow Solid or liquid
PURITY 94.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿6,730.00
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0.250 10-20 days ฿13,800.00
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1.000 10-20 days ฿30,240.00
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1-((2-(Trimethylsilyl)Ethoxy)Methyl)-1H-1,2,4-Triazole
This chemical is primarily used in organic synthesis as a protecting group for alcohols and other functional groups. Its trimethylsilyl ethoxymethyl (SEM) group is effective in shielding reactive sites during complex chemical reactions, particularly in the synthesis of pharmaceuticals and fine chemicals. The SEM group is stable under various reaction conditions but can be selectively removed under mild acidic conditions, making it a versatile tool in multi-step synthetic processes. Additionally, it finds application in the preparation of heterocyclic compounds, where it aids in controlling the reactivity and selectivity of intermediates. Its utility in peptide synthesis and the development of bioactive molecules further highlights its importance in medicinal chemistry.
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