tert-Butyl (3-(hydroxymethyl)phenyl)carbamate
97%
- Product Code: 113192
CAS:
118684-31-4
| Molecular Weight: | 223.27 g./mol | Molecular Formula: | C₁₂H₁₇NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04974269 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis as a protective group for amines. The tert-butyl carbamate moiety is particularly effective in safeguarding the amine functionality during multi-step synthetic processes, especially in the preparation of complex molecules such as pharmaceuticals and agrochemicals. Its stability under various reaction conditions allows for selective deprotection when needed, making it a valuable tool in the development of active pharmaceutical ingredients (APIs). Additionally, the hydroxymethyl group on the phenyl ring provides a reactive site for further functionalization, enabling the attachment of other chemical groups to create diverse derivatives. This versatility makes it a useful intermediate in the synthesis of biologically active compounds, including potential drug candidates.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Solid |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,360.00 |
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| 1.000 | 10-20 days | ฿5,250.00 |
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| 5.000 | 10-20 days | ฿12,060.00 |
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| 10.000 | 10-20 days | ฿19,044.00 |
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tert-Butyl (3-(hydroxymethyl)phenyl)carbamate
This compound is primarily utilized in organic synthesis as a protective group for amines. The tert-butyl carbamate moiety is particularly effective in safeguarding the amine functionality during multi-step synthetic processes, especially in the preparation of complex molecules such as pharmaceuticals and agrochemicals. Its stability under various reaction conditions allows for selective deprotection when needed, making it a valuable tool in the development of active pharmaceutical ingredients (APIs). Additionally, the hydroxymethyl group on the phenyl ring provides a reactive site for further functionalization, enabling the attachment of other chemical groups to create diverse derivatives. This versatility makes it a useful intermediate in the synthesis of biologically active compounds, including potential drug candidates.
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