((3S,4S)-4-Methylpyrrolidin-3-yl)methanol
98%
- Product Code: 84756
CAS:
1279034-51-3
Molecular Weight: | 115.17 g./mol | Molecular Formula: | C₆H₁₃NO |
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EC Number: | MDL Number: | MFCD11559112 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various therapeutic agents. Its structural properties make it valuable for the development of drugs targeting neurological disorders, particularly those involving dopamine regulation. It is often incorporated into the synthesis of compounds that act as dopamine reuptake inhibitors or receptor modulators, which are essential in treating conditions like Parkinson’s disease, depression, and ADHD. Additionally, its chiral centers allow for the creation of enantiomerically pure substances, enhancing the specificity and efficacy of the resulting drugs. Researchers also explore its potential in designing novel antiviral and anticancer agents due to its ability to interact with biological targets selectively.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿27,180.00 |
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((3S,4S)-4-Methylpyrrolidin-3-yl)methanol
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various therapeutic agents. Its structural properties make it valuable for the development of drugs targeting neurological disorders, particularly those involving dopamine regulation. It is often incorporated into the synthesis of compounds that act as dopamine reuptake inhibitors or receptor modulators, which are essential in treating conditions like Parkinson’s disease, depression, and ADHD. Additionally, its chiral centers allow for the creation of enantiomerically pure substances, enhancing the specificity and efficacy of the resulting drugs. Researchers also explore its potential in designing novel antiviral and anticancer agents due to its ability to interact with biological targets selectively.
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