1,3-Pyrrolidinedicarboxylic acid, 4-ethyl-, 1-(1,1-dimethylethyl) ester

95%

Reagent Code: #226468
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CAS Number 1779899-46-5

science Other reagents with same CAS 1779899-46-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.29944 g/mol
Formula C₁₂H₂₁NO₄
badge Registry Numbers
MDL Number MFCD18073852
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its protected carboxylic acid group and chiral structure make it valuable in developing active pharmaceutical ingredients (APIs), especially in the design of peptidomimetics and enzyme inhibitors. The tert-butyl ester group allows for selective deprotection, enabling stepwise synthesis in multi-step reactions. Commonly applied in research settings for drug discovery and development.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿4,550.00
1g
10-20 days ฿11,680.00
1,3-Pyrrolidinedicarboxylic acid, 4-ethyl-, 1-(1,1-dimethylethyl) ester
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Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its protected carboxylic acid group and chiral structure make it valuable in developing active pharmaceutical ingredients (APIs), especially in the design of peptidomimetics and enzyme inhibitors. The tert-butyl ester group allows for selective deprotection, enabling stepwise synthesis in multi-step reactions. Commonly applied in research settings for drug discovery and developmen

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its protected carboxylic acid group and chiral structure make it valuable in developing active pharmaceutical ingredients (APIs), especially in the design of peptidomimetics and enzyme inhibitors. The tert-butyl ester group allows for selective deprotection, enabling stepwise synthesis in multi-step reactions. Commonly applied in research settings for drug discovery and development.

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