(S)-1-(3-Chloro-5-fluorophenyl)ethanamine hydrochloride
97%
- Product Code: 113654
CAS:
1998701-29-3
Molecular Weight: | 210.08 g./mol | Molecular Formula: | C₈H₁₀Cl₂FN |
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EC Number: | MDL Number: | MFCD12758064 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the production of enantiomerically pure drugs, particularly those targeting neurological and psychiatric disorders. The presence of both chloro and fluoro substituents enhances its binding affinity to specific biological targets, making it useful in the development of receptor-specific medications. Additionally, it is employed in research settings for the study of enzyme interactions and the development of novel therapeutic agents. Its hydrochloride form ensures stability and solubility, facilitating its use in various formulations and experimental protocols.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿6,372.00 |
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0.250 | 10-20 days | ฿8,145.00 |
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(S)-1-(3-Chloro-5-fluorophenyl)ethanamine hydrochloride
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the production of enantiomerically pure drugs, particularly those targeting neurological and psychiatric disorders. The presence of both chloro and fluoro substituents enhances its binding affinity to specific biological targets, making it useful in the development of receptor-specific medications. Additionally, it is employed in research settings for the study of enzyme interactions and the development of novel therapeutic agents. Its hydrochloride form ensures stability and solubility, facilitating its use in various formulations and experimental protocols.
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