((2S,4S)-1-benzyl-4-((tert-butyldimethylsilyl)oxy)pyrrolidin-2-yl)methanol
98%
- Product Code: 123580
CAS:
635299-82-0
Molecular Weight: | 321.53 g./mol | Molecular Formula: | C₁₈H₃₁NO₂Si |
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EC Number: | MDL Number: | MFCD29472563 | |
Melting Point: | Boiling Point: | 375.3±32.0 °C(Predicted) | |
Density: | 1.02±0.1 g/cm3(Predicted) | Storage Condition: | room temperature, dry, sealed |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of complex molecules, particularly in the pharmaceutical industry. It is often employed in the synthesis of chiral compounds due to its stereochemical configuration, which can influence the stereoselectivity of reactions. The tert-butyldimethylsilyl (TBDMS) group serves as a protective group for the hydroxyl moiety, allowing for selective reactions at other functional sites. This compound is also used in the development of bioactive molecules, including potential drug candidates, where the pyrrolidine ring structure is a key scaffold. Its application extends to peptide synthesis and the creation of novel materials with specific stereochemical properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿19,971.00 |
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1.000 | 10-20 days | ฿39,942.00 |
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((2S,4S)-1-benzyl-4-((tert-butyldimethylsilyl)oxy)pyrrolidin-2-yl)methanol
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of complex molecules, particularly in the pharmaceutical industry. It is often employed in the synthesis of chiral compounds due to its stereochemical configuration, which can influence the stereoselectivity of reactions. The tert-butyldimethylsilyl (TBDMS) group serves as a protective group for the hydroxyl moiety, allowing for selective reactions at other functional sites. This compound is also used in the development of bioactive molecules, including potential drug candidates, where the pyrrolidine ring structure is a key scaffold. Its application extends to peptide synthesis and the creation of novel materials with specific stereochemical properties.
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