(S)-1-(3-Bromophenyl)propan-1-amine hydrochloride
97%
- Product Code: 37903
CAS:
623143-34-0
| Molecular Weight: | 250.56 g./mol | Molecular Formula: | C₉H₁₃BrClN |
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| EC Number: | MDL Number: | MFCD12756925 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring a bromophenyl group and an amine functionality, makes it a valuable intermediate in the creation of biologically active compounds. It is often employed in the design and production of drugs targeting the central nervous system, where its chiral nature can influence receptor binding and efficacy. Additionally, it serves as a building block in organic synthesis for the preparation of more complex molecules, including potential therapeutic agents and ligands for asymmetric catalysis. Its applications are particularly relevant in medicinal chemistry, where it aids in the exploration of new drug candidates with improved selectivity and potency.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $205.57 |
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| 0.250 | 10-20 days | $411.14 |
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(S)-1-(3-Bromophenyl)propan-1-amine hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring a bromophenyl group and an amine functionality, makes it a valuable intermediate in the creation of biologically active compounds. It is often employed in the design and production of drugs targeting the central nervous system, where its chiral nature can influence receptor binding and efficacy. Additionally, it serves as a building block in organic synthesis for the preparation of more complex molecules, including potential therapeutic agents and ligands for asymmetric catalysis. Its applications are particularly relevant in medicinal chemistry, where it aids in the exploration of new drug candidates with improved selectivity and potency.
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