((2S,4S)-1-benzyl-4-((tert-butyldimethylsilyl)oxy)pyrrolidin-2-yl)methanol

98%

Reagent Code: #123580
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CAS Number 635299-82-0

science Other reagents with same CAS 635299-82-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.53 g/mol
Formula C₁₈H₃₁NO₂Si
badge Registry Numbers
MDL Number MFCD29472563
thermostat Physical Properties
Boiling Point 375.3±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.02±0.1 g/cm3(Predicted)
Storage room temperature, dry, sealed

description 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.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿19,971.00
inventory 1g
10-20 days ฿39,942.00

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((2S,4S)-1-benzyl-4-((tert-butyldimethylsilyl)oxy)pyrrolidin-2-yl)methanol
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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 d

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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