4-((tert-Butyldimethylsilyloxy)methyl)aniline
95%
- Product Code: 46048
CAS:
131230-76-7
| Molecular Weight: | 237.41 g./mol | Molecular Formula: | C₁₃H₂₃NOSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20483304 | |
| Melting Point: | Boiling Point: | 305.0±17.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily used in organic synthesis as a protected intermediate for the preparation of more complex molecules. Its tert-butyldimethylsilyl (TBDMS) group serves as a protective group for hydroxyl functionalities, ensuring stability during reactions. It is particularly valuable in the synthesis of pharmaceuticals, where selective protection and deprotection of functional groups are crucial. Additionally, it can be employed in the development of organic materials, such as polymers or dyes, where controlled reactivity is essential. Its application extends to research settings, where it aids in the study of reaction mechanisms and the development of novel synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,052.00 |
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| 0.250 | 10-20 days | ฿3,582.00 |
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| 1.000 | 10-20 days | ฿8,946.00 |
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| 5.000 | 10-20 days | ฿28,755.00 |
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4-((tert-Butyldimethylsilyloxy)methyl)aniline
This chemical is primarily used in organic synthesis as a protected intermediate for the preparation of more complex molecules. Its tert-butyldimethylsilyl (TBDMS) group serves as a protective group for hydroxyl functionalities, ensuring stability during reactions. It is particularly valuable in the synthesis of pharmaceuticals, where selective protection and deprotection of functional groups are crucial. Additionally, it can be employed in the development of organic materials, such as polymers or dyes, where controlled reactivity is essential. Its application extends to research settings, where it aids in the study of reaction mechanisms and the development of novel synthetic pathways.
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