(R)-tert-Butyl (1-(4-bromophenyl)-2-hydroxyethyl)carbamate
97%
- Product Code: 37271
CAS:
849178-85-4
| Molecular Weight: | 316.19 g./mol | Molecular Formula: | C₁₃H₁₈BrNO₃ |
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| EC Number: | MDL Number: | MFCD28148212 | |
| Melting Point: | Boiling Point: | 438.3±40.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis as a chiral intermediate for the production of pharmaceuticals and biologically active molecules. Its structure, featuring a bromophenyl group and a hydroxyl group, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological disorders and cancer. The tert-butyl carbamate group acts as a protective group for amines, allowing selective reactions to occur at other functional sites. Additionally, its chiral nature is crucial for synthesizing enantiomerically pure compounds, which are often required for effective and safe therapeutic agents. It is also employed in research settings for studying enzyme inhibition and receptor binding mechanisms due to its specific stereochemistry and functional groups.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $120.69 |
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| 0.250 | 10-20 days | $217.43 |
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| 1.000 | 10-20 days | $587.64 |
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(R)-tert-Butyl (1-(4-bromophenyl)-2-hydroxyethyl)carbamate
This compound is primarily utilized in organic synthesis as a chiral intermediate for the production of pharmaceuticals and biologically active molecules. Its structure, featuring a bromophenyl group and a hydroxyl group, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological disorders and cancer. The tert-butyl carbamate group acts as a protective group for amines, allowing selective reactions to occur at other functional sites. Additionally, its chiral nature is crucial for synthesizing enantiomerically pure compounds, which are often required for effective and safe therapeutic agents. It is also employed in research settings for studying enzyme inhibition and receptor binding mechanisms due to its specific stereochemistry and functional groups.
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