1,2-Pyrrolidinedicarboxylicacid, 4-hydroxy-5-oxo-, 1-(1,1-dimethylethyl) 2-methyl ester, (2S,4R)-

≥95%

Reagent Code: #223299
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CAS Number 367966-41-4

science Other reagents with same CAS 367966-41-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.2558 g/mol
Formula C₁₁H₁₇NO₆
badge Registry Numbers
MDL Number MFCD08274462
thermostat Physical Properties
Melting Point 90-92 °C
Boiling Point 412.6±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.309±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors. Its stereochemistry makes it valuable for creating biologically active molecules with high enantioselectivity. Commonly employed in research settings for constructing complex organic compounds, especially those requiring defined spatial orientation of functional groups. The protected carboxylic acid groups allow for selective deprotection and further derivatization in multi-step synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿14,770.00
250mg
10-20 days ฿24,720.00
1g
10-20 days ฿61,780.00
1,2-Pyrrolidinedicarboxylicacid, 4-hydroxy-5-oxo-, 1-(1,1-dimethylethyl) 2-methyl ester, (2S,4R)-
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors. Its stereochemistry makes it valuable for creating biologically active molecules with high enantioselectivity. Commonly employed in research settings for constructing complex organic compounds, especially those requiring defined spatial orientation of functional groups. The protected carboxylic acid groups allow for selective deprotection and further derivatization in multi-step sy

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors. Its stereochemistry makes it valuable for creating biologically active molecules with high enantioselectivity. Commonly employed in research settings for constructing complex organic compounds, especially those requiring defined spatial orientation of functional groups. The protected carboxylic acid groups allow for selective deprotection and further derivatization in multi-step synthesis.

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