(3R,4S)-4-(3-Chlorophenyl)pyrrolidine-3-carboxylic acid
≥95%
- Product Code: 36758
CAS:
1047651-80-8
Molecular Weight: | 225.67 g./mol | Molecular Formula: | C₁₁H₁₂ClNO₂ |
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EC Number: | MDL Number: | MFCD11520170 | |
Melting Point: | Boiling Point: | 399°C at 760 mmHg | |
Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of pharmaceutical agents. Its structure, featuring a pyrrolidine ring and a chlorophenyl group, makes it valuable for designing molecules that target specific biological pathways. It is often employed in the development of drugs aimed at treating neurological disorders, such as Parkinson's disease or schizophrenia, due to its potential interactions with neurotransmitter systems. Additionally, its chiral centers allow for the creation of enantiomerically pure compounds, which are crucial for optimizing drug efficacy and minimizing side effects. Researchers also explore its use in creating ligands for receptors involved in pain management and inflammation.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $38.58 |
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0.250 | 10-20 days | $77.51 |
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(3R,4S)-4-(3-Chlorophenyl)pyrrolidine-3-carboxylic acid
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of pharmaceutical agents. Its structure, featuring a pyrrolidine ring and a chlorophenyl group, makes it valuable for designing molecules that target specific biological pathways. It is often employed in the development of drugs aimed at treating neurological disorders, such as Parkinson's disease or schizophrenia, due to its potential interactions with neurotransmitter systems. Additionally, its chiral centers allow for the creation of enantiomerically pure compounds, which are crucial for optimizing drug efficacy and minimizing side effects. Researchers also explore its use in creating ligands for receptors involved in pain management and inflammation.
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