(2S,4S)-1-tert-butyl 2-methyl 4-(hydroxymethyl)pyrrolidine-1,2-dicarboxylate

97%

Reagent Code: #232857
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CAS Number 1194059-42-1

science Other reagents with same CAS 1194059-42-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.2988 g/mol
Formula C₁₂H₂₁NO₅
badge Registry Numbers
MDL Number MFCD28502697
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in medicinal chemistry for constructing complex cyclic structures with defined spatial orientation. Also utilized in the preparation of peptidomimetics due to the pyrrolidine backbone mimicking natural amino acid conformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,200.00
inventory 250mg
10-20 days ฿14,400.00
inventory 500mg
10-20 days ฿24,000.00
(2S,4S)-1-tert-butyl 2-methyl 4-(hydroxymethyl)pyrrolidine-1,2-dicarboxylate
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Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in medicinal chemistry for constructing complex cyclic structures with defined spatial orientation. Also utilized in the preparation of peptidomimetics due to the pyrrolidine backbone mimicking

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in medicinal chemistry for constructing complex cyclic structures with defined spatial orientation. Also utilized in the preparation of peptidomimetics due to the pyrrolidine backbone mimicking natural amino acid conformations.

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