1-(Tert-butyl) 2-methyl (2S)-5-allylpyrrolidine-1,2-dicarboxylate

95%

Reagent Code: #82991
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CAS Number 195964-65-9

science Other reagents with same CAS 195964-65-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.34 g/mol
Formula C₁₄H₂₃NO₄
badge Registry Numbers
MDL Number MFCD16877486
thermostat Physical Properties
Boiling Point 328.9±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.061±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis as a chiral building block. Its structure, featuring both a tert-butyl group and an allyl group, makes it valuable in the preparation of complex molecules, particularly in pharmaceutical research. The compound is often employed in the synthesis of pyrrolidine-based frameworks, which are common in bioactive molecules and drug candidates. Its stereochemistry allows for the creation of enantiomerically pure products, which is crucial in the development of therapeutic agents with specific biological activities. Additionally, the allyl group provides a handle for further functionalization through reactions like cross-coupling or olefin metathesis, enhancing its versatility in synthetic applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,360.00
inventory 250mg
10-20 days ฿17,550.00
inventory 1g
10-20 days ฿35,100.00

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1-(Tert-butyl) 2-methyl (2S)-5-allylpyrrolidine-1,2-dicarboxylate
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This compound is primarily utilized in organic synthesis as a chiral building block. Its structure, featuring both a tert-butyl group and an allyl group, makes it valuable in the preparation of complex molecules, particularly in pharmaceutical research. The compound is often employed in the synthesis of pyrrolidine-based frameworks, which are common in bioactive molecules and drug candidates. Its stereochemistry allows for the creation of enantiomerically pure products, which is crucial in the developmen

This compound is primarily utilized in organic synthesis as a chiral building block. Its structure, featuring both a tert-butyl group and an allyl group, makes it valuable in the preparation of complex molecules, particularly in pharmaceutical research. The compound is often employed in the synthesis of pyrrolidine-based frameworks, which are common in bioactive molecules and drug candidates. Its stereochemistry allows for the creation of enantiomerically pure products, which is crucial in the development of therapeutic agents with specific biological activities. Additionally, the allyl group provides a handle for further functionalization through reactions like cross-coupling or olefin metathesis, enhancing its versatility in synthetic applications.

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