(1S,2S)-rel-2-(4-Hydroxyphenyl)cyclopropane-1-carboxylic acid
97%
- Product Code: 232523
CAS:
731810-73-4
| Molecular Weight: | 178.18 g./mol | Molecular Formula: | C₁₀H₁₀O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29918582 | |
| Melting Point: | Boiling Point: | 393.4±42.0 °C(Predicted) | |
| Density: | 1.390±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its rigid cyclopropane scaffold and defined stereochemistry enhance binding selectivity and metabolic stability in drug candidates. It is also employed in the preparation of bioactive molecules where stereochemical control is critical for activity. The phenolic hydroxyl group allows for further functionalization, such as glycosylation or ether formation, enabling structural diversification for structure-activity relationship (SAR) studies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | $725.38 |
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| 1.000 | 10-20 days | $1,087.81 |
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(1S,2S)-rel-2-(4-Hydroxyphenyl)cyclopropane-1-carboxylic acid
Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its rigid cyclopropane scaffold and defined stereochemistry enhance binding selectivity and metabolic stability in drug candidates. It is also employed in the preparation of bioactive molecules where stereochemical control is critical for activity. The phenolic hydroxyl group allows for further functionalization, such as glycosylation or ether formation, enabling structural diversification for structure-activity relationship (SAR) studies.
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