(R)-(-)-N-BOC-3-pyrrolidinol
98%
- Product Code: 229881
Alias:
(R)-1-Boc-3-hydroxypyrrolidine; (R)-1-(tert-butoxycarbonyl)-3-pyrrolidine alcohol
CAS:
109431-87-0
Molecular Weight: | 187.24 g./mol | Molecular Formula: | C₉H₁₇NO₃ |
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EC Number: | MDL Number: | MFCD01317838 | |
Melting Point: | 62-65 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected alcohol and amine functionalities make it ideal for sequential coupling reactions in multi-step organic syntheses. Commonly employed in the production of neuroactive drugs, antivirals, and enzyme inhibitors where the (R)-enantiomer provides optimal biological activity. The BOC-protected amine allows for easy deprotection under mild acidic conditions, enabling further functionalization without racemization. Widely utilized in research and industrial settings for combinatorial chemistry and high-throughput screening of drug candidates.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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0.250 | 10-20 days | $9.06 |
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1.000 | 10-20 days | $9.37 |
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5.000 | 10-20 days | $17.18 |
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25.000 | 10-20 days | $49.45 |
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500.000 | 10-20 days | $860.44 |
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100.000 | 10-20 days | $174.38 |
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(R)-(-)-N-BOC-3-pyrrolidinol
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected alcohol and amine functionalities make it ideal for sequential coupling reactions in multi-step organic syntheses. Commonly employed in the production of neuroactive drugs, antivirals, and enzyme inhibitors where the (R)-enantiomer provides optimal biological activity. The BOC-protected amine allows for easy deprotection under mild acidic conditions, enabling further functionalization without racemization. Widely utilized in research and industrial settings for combinatorial chemistry and high-throughput screening of drug candidates.
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