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 |
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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 |
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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 |
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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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