Bromotrimethylsilane
98%
- Product Code: 88321
Alias:
Trimethylbromosilane
CAS:
2857-97-8
Molecular Weight: | 153.09 g./mol | Molecular Formula: | C₃H₉BrSi |
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EC Number: | 220-672-0 | MDL Number: | MFCD00000048 |
Melting Point: | -43 °C | Boiling Point: | 79 °C(lit.) |
Density: | 1.16 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C |
Product Description:
Bromotrimethylsilane is widely used in organic synthesis as a reagent for introducing the trimethylsilyl group into molecules. It is particularly effective in protecting alcohols and phenols by converting them into their corresponding trimethylsilyl ethers, which are stable under various reaction conditions. This protection allows for selective reactions to be carried out on other functional groups within the molecule. Additionally, it is employed in the cleavage of ethers, especially methyl ethers, facilitating the deprotection of hydroxyl groups. In peptide synthesis, it serves as a deprotecting agent for tert-butyl esters and ethers, enabling the formation of complex peptide structures. Its role in the synthesis of silicon-containing compounds is also notable, contributing to the development of materials with unique properties.
Product Specification:
Test | Specification |
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PurityGC | 98-100 |
REFRACTIVE INDEX N20D | 1.42-1.425 |
SPECIFIC GRAVITY 2020C | 1.17-1.2 |
APPEARANCE | Colorless to light yellow liquid |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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25.000 | 10-20 days | $27.71 |
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100.000 | 10-20 days | $70.92 |
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500.000 | 10-20 days | $241.86 |
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2500.000 | 10-20 days | $1,032.74 |
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Bromotrimethylsilane
Bromotrimethylsilane is widely used in organic synthesis as a reagent for introducing the trimethylsilyl group into molecules. It is particularly effective in protecting alcohols and phenols by converting them into their corresponding trimethylsilyl ethers, which are stable under various reaction conditions. This protection allows for selective reactions to be carried out on other functional groups within the molecule. Additionally, it is employed in the cleavage of ethers, especially methyl ethers, facilitating the deprotection of hydroxyl groups. In peptide synthesis, it serves as a deprotecting agent for tert-butyl esters and ethers, enabling the formation of complex peptide structures. Its role in the synthesis of silicon-containing compounds is also notable, contributing to the development of materials with unique properties.
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