(R)-tert-Butyl (1-(3-chlorophenyl)-2-hydroxyethyl)carbamate
97%
- Product Code: 113598
CAS:
926291-64-7
| Molecular Weight: | 271.74 g./mol | Molecular Formula: | C₁₃H₁₈ClNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD25977349 | |
| Melting Point: | Boiling Point: | 405.9±40.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules. Its structure, featuring a chiral center and functional groups like the carbamate and hydroxyl, makes it valuable for developing enantiomerically pure drugs. It is often employed in the production of β-blockers, which are medications used to manage cardiovascular conditions such as hypertension and arrhythmias. Additionally, its chlorophenyl group contributes to its role in creating compounds with potential biological activity, including anti-inflammatory or antimicrobial agents. The tert-butyl group enhances stability, making it suitable for use in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,980.00 |
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| 0.250 | 10-20 days | ฿2,961.00 |
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| 1.000 | 10-20 days | ฿7,434.00 |
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| 5.000 | 10-20 days | ฿22,311.00 |
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(R)-tert-Butyl (1-(3-chlorophenyl)-2-hydroxyethyl)carbamate
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules. Its structure, featuring a chiral center and functional groups like the carbamate and hydroxyl, makes it valuable for developing enantiomerically pure drugs. It is often employed in the production of β-blockers, which are medications used to manage cardiovascular conditions such as hypertension and arrhythmias. Additionally, its chlorophenyl group contributes to its role in creating compounds with potential biological activity, including anti-inflammatory or antimicrobial agents. The tert-butyl group enhances stability, making it suitable for use in multi-step synthetic processes.
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