tert-Butyldimethyl(prop-2-ynyloxy)silane
97%
- Product Code: 88531
Alias:
(propargyloxy) tert-butyldimethylsilane;
CAS:
76782-82-6
| Molecular Weight: | 170.32 g./mol | Molecular Formula: | C₉H₁₈OSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01863574 | |
| Melting Point: | Boiling Point: | 157.8ºC | |
| Density: | 0.838 g/cm3 | Storage Condition: | 2~8°C, sealed |
Product Description:
This chemical is primarily used as a protecting group in organic synthesis, particularly for alcohols. Its application is significant in the preparation of complex molecules, where it helps to shield hydroxyl groups during reactions that might otherwise affect them. The compound is also utilized in the synthesis of alkynes, where it acts as a precursor or intermediate. Its stability and ease of removal under mild conditions make it a valuable tool in peptide and carbohydrate chemistry. Additionally, it finds use in the development of pharmaceuticals and agrochemicals, where selective protection and deprotection of functional groups are crucial.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 96.5-100 |
| Appearance | Colorless to light yellow liquid |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿1,860.00 |
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| 25.000 | 10-20 days | ฿6,860.00 |
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| 100.000 | 10-20 days | ฿21,780.00 |
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tert-Butyldimethyl(prop-2-ynyloxy)silane
This chemical is primarily used as a protecting group in organic synthesis, particularly for alcohols. Its application is significant in the preparation of complex molecules, where it helps to shield hydroxyl groups during reactions that might otherwise affect them. The compound is also utilized in the synthesis of alkynes, where it acts as a precursor or intermediate. Its stability and ease of removal under mild conditions make it a valuable tool in peptide and carbohydrate chemistry. Additionally, it finds use in the development of pharmaceuticals and agrochemicals, where selective protection and deprotection of functional groups are crucial.
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