1-((Trimethylsilyl)methyl)-1H-benzo[d][1,2,3]triazole
97%
- Product Code: 192222
CAS:
122296-00-8
| Molecular Weight: | 205.33 g./mol | Molecular Formula: | C₁₀H₁₅N₃Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00956443 | |
| Melting Point: | 56-60 °C(lit.) | Boiling Point: | 300.3±25.0 °C(Predicted) |
| Density: | 1.06±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, seal, inert gas |
Product Description:
Used as a reagent in organic synthesis, particularly in cross-coupling reactions where the trimethylsilylmethyl group acts as a masked functional group or stabilizing moiety. It serves as a benzotriazole derivative that can participate in palladium-catalyzed transformations, enabling the formation of carbon-nitrogen or carbon-carbon bonds in pharmaceutical and agrochemical intermediates. Its silyl group enhances lipophilicity and can improve substrate solubility in nonpolar reaction media. Also employed in the development of functional materials due to its stability and ability to undergo selective deprotection or transformation under mild conditions.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿1,150.00 |
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| 1.000 G | 10-20 days | ฿3,490.00 |
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| 5.000 G | 10-20 days | ฿11,990.00 |
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1-((Trimethylsilyl)methyl)-1H-benzo[d][1,2,3]triazole
Used as a reagent in organic synthesis, particularly in cross-coupling reactions where the trimethylsilylmethyl group acts as a masked functional group or stabilizing moiety. It serves as a benzotriazole derivative that can participate in palladium-catalyzed transformations, enabling the formation of carbon-nitrogen or carbon-carbon bonds in pharmaceutical and agrochemical intermediates. Its silyl group enhances lipophilicity and can improve substrate solubility in nonpolar reaction media. Also employed in the development of functional materials due to its stability and ability to undergo selective deprotection or transformation under mild conditions.
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