(R)-2-Amino-2-(4-bromophenyl)ethanol
≥95%
- Product Code: 113518
CAS:
354153-64-3
Molecular Weight: | 216.08 g./mol | Molecular Formula: | C₈H₁₀BrNO |
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EC Number: | MDL Number: | MFCD09256373 | |
Melting Point: | Boiling Point: | 341.6±27.0°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
(R)-2-Amino-2-(4-bromophenyl)ethanol is primarily utilized in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of enantiomerically pure drugs, which are crucial for ensuring high efficacy and minimizing side effects. This compound is often employed in the development of beta-blockers, a class of medications used to manage cardiovascular conditions such as hypertension and arrhythmias. Additionally, it finds application in the creation of ligands for asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions in organic synthesis. Its role in constructing complex molecular architectures makes it valuable in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $78.57 |
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0.250 | 10-20 days | $96.27 |
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(R)-2-Amino-2-(4-bromophenyl)ethanol
(R)-2-Amino-2-(4-bromophenyl)ethanol is primarily utilized in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of enantiomerically pure drugs, which are crucial for ensuring high efficacy and minimizing side effects. This compound is often employed in the development of beta-blockers, a class of medications used to manage cardiovascular conditions such as hypertension and arrhythmias. Additionally, it finds application in the creation of ligands for asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions in organic synthesis. Its role in constructing complex molecular architectures makes it valuable in medicinal chemistry and drug discovery processes.
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