(S)-1-(4-(Cyclopentyloxy)phenyl)ethan-1-amine hydrochloride
95%
- Product Code: 233395
CAS:
2703745-89-3
| Molecular Weight: | 241.76 g./mol | Molecular Formula: | C₁₃H₂₀ClNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32062641 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, light-proof, inert gas |
Product Description:
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as an intermediate in the production of selective serotonin reuptake inhibitors (SSRIs) and other bioactive molecules where the (S)-enantiomer contributes to desired pharmacological activity. Its amine functionality allows for coupling reactions, while the cyclopentyloxy aromatic group provides structural similarity to known drug scaffolds, enhancing binding affinity to specific receptors. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $1,418.06 |
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| 0.250 | 10-20 days | $2,126.06 |
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| 1.000 | 10-20 days | $5,311.79 |
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(S)-1-(4-(Cyclopentyloxy)phenyl)ethan-1-amine hydrochloride
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as an intermediate in the production of selective serotonin reuptake inhibitors (SSRIs) and other bioactive molecules where the (S)-enantiomer contributes to desired pharmacological activity. Its amine functionality allows for coupling reactions, while the cyclopentyloxy aromatic group provides structural similarity to known drug scaffolds, enhancing binding affinity to specific receptors. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies.
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