(R)-3-(1-Aminoethyl)benzoic acid hydrochloride
95%
- Product Code: 55894
CAS:
1391437-37-8
| Molecular Weight: | 201.6501 g./mol | Molecular Formula: | C₉H₁₂ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12757355 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
(R)-3-(1-Aminoethyl)benzoic acid hydrochloride is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its enantiomeric purity makes it valuable in the production of drugs that require specific stereochemistry to achieve desired therapeutic effects. It is often employed in the development of compounds targeting neurological and cardiovascular disorders, where precise molecular configuration is critical for efficacy and safety. Additionally, it serves as an intermediate in the synthesis of complex organic molecules, enabling the creation of more potent and selective drug candidates. Its application extends to research and development, where it aids in the exploration of new drug pathways and mechanisms.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿12,960.00 |
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(R)-3-(1-Aminoethyl)benzoic acid hydrochloride
(R)-3-(1-Aminoethyl)benzoic acid hydrochloride is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its enantiomeric purity makes it valuable in the production of drugs that require specific stereochemistry to achieve desired therapeutic effects. It is often employed in the development of compounds targeting neurological and cardiovascular disorders, where precise molecular configuration is critical for efficacy and safety. Additionally, it serves as an intermediate in the synthesis of complex organic molecules, enabling the creation of more potent and selective drug candidates. Its application extends to research and development, where it aids in the exploration of new drug pathways and mechanisms.
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