tert-Butyl N-(2-bromoethyl)carbamate
98%
- Product Code: 72784
Alias:
2-(Boc-amino)ethyl bromide; tert-butyl N-(2-bromoethyl)carbamate
CAS:
39684-80-5
| Molecular Weight: | 224.10 g./mol | Molecular Formula: | C₇H₁₄BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02683428 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20℃ |
Product Description:
This chemical is primarily used in organic synthesis as a protective group for amines. The tert-butyl carbamate (Boc) group shields the amine functionality during multi-step reactions, allowing selective transformations to occur elsewhere in the molecule. The 2-bromoethyl moiety provides a reactive site for further functionalization, such as nucleophilic substitution or coupling reactions. It is particularly valuable in peptide synthesis and the preparation of complex organic molecules, where protecting groups are essential to control reactivity and achieve desired outcomes. Additionally, it serves as an intermediate in the development of pharmaceuticals, agrochemicals, and other fine chemicals.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98-100 |
| Melting point | 28-33 |
| Appearance | white to beige Low melting solid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿420.00 |
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| 5.000 | 10-20 days | ฿1,080.00 |
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| 25.000 | 10-20 days | ฿3,980.00 |
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| 100.000 | 10-20 days | ฿14,900.00 |
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tert-Butyl N-(2-bromoethyl)carbamate
This chemical is primarily used in organic synthesis as a protective group for amines. The tert-butyl carbamate (Boc) group shields the amine functionality during multi-step reactions, allowing selective transformations to occur elsewhere in the molecule. The 2-bromoethyl moiety provides a reactive site for further functionalization, such as nucleophilic substitution or coupling reactions. It is particularly valuable in peptide synthesis and the preparation of complex organic molecules, where protecting groups are essential to control reactivity and achieve desired outcomes. Additionally, it serves as an intermediate in the development of pharmaceuticals, agrochemicals, and other fine chemicals.
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