(S)-tert-Butyl (1-(2-bromophenyl)ethyl)carbamate
≥95%
- Product Code: 113633
CAS:
1187932-11-1
| Molecular Weight: | 300.19 g./mol | Molecular Formula: | C₁₃H₁₈BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11506016 | |
| Melting Point: | Boiling Point: | 375.2±25.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of chiral compounds, where its stereochemistry plays a crucial role in creating enantiomerically pure drugs. The presence of the bromophenyl group allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, making it a versatile building block in medicinal chemistry. Additionally, the tert-butyl carbamate group provides a protective function for amines, enabling selective reactions in multi-step synthetic processes. Its application is also seen in the synthesis of biologically active compounds, including potential therapeutic agents targeting neurological disorders or cancer.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,851.00 |
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| 0.250 | 10-20 days | ฿7,281.00 |
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| 1.000 | 10-20 days | ฿16,731.00 |
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(S)-tert-Butyl (1-(2-bromophenyl)ethyl)carbamate
This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of chiral compounds, where its stereochemistry plays a crucial role in creating enantiomerically pure drugs. The presence of the bromophenyl group allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, making it a versatile building block in medicinal chemistry. Additionally, the tert-butyl carbamate group provides a protective function for amines, enabling selective reactions in multi-step synthetic processes. Its application is also seen in the synthesis of biologically active compounds, including potential therapeutic agents targeting neurological disorders or cancer.
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