(2S,4R)-Di-tert-Butyl 4-hydroxypyrrolidine-1,2-dicarboxylate

95%

Reagent Code: #104156
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CAS Number 170850-75-6

science Other reagents with same CAS 170850-75-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.35 g/mol
Formula C₁₄H₂₅NO₅
badge Registry Numbers
MDL Number MFCD01318729
thermostat Physical Properties
Melting Point 62-64 °C
Boiling Point 369.1±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.144±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized as an intermediate in the synthesis of more complex molecules, particularly in the pharmaceutical industry. It plays a crucial role in the development of chiral drugs, where its stereochemistry is essential for producing enantiomerically pure substances. The compound is often employed in the preparation of pyrrolidine-based frameworks, which are common in bioactive molecules and therapeutic agents. Its hydroxyl and carboxylate groups make it a versatile building block for constructing drug candidates, especially those targeting neurological and cardiovascular diseases. Additionally, it is used in research settings to study stereochemical effects in organic reactions and to develop new synthetic methodologies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,860.00
inventory 1g
10-20 days ฿12,150.00
inventory 100mg
10-20 days ฿2,700.00

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(2S,4R)-Di-tert-Butyl 4-hydroxypyrrolidine-1,2-dicarboxylate
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This compound is primarily utilized as an intermediate in the synthesis of more complex molecules, particularly in the pharmaceutical industry. It plays a crucial role in the development of chiral drugs, where its stereochemistry is essential for producing enantiomerically pure substances. The compound is often employed in the preparation of pyrrolidine-based frameworks, which are common in bioactive molecules and therapeutic agents. Its hydroxyl and carboxylate groups make it a versatile building block

This compound is primarily utilized as an intermediate in the synthesis of more complex molecules, particularly in the pharmaceutical industry. It plays a crucial role in the development of chiral drugs, where its stereochemistry is essential for producing enantiomerically pure substances. The compound is often employed in the preparation of pyrrolidine-based frameworks, which are common in bioactive molecules and therapeutic agents. Its hydroxyl and carboxylate groups make it a versatile building block for constructing drug candidates, especially those targeting neurological and cardiovascular diseases. Additionally, it is used in research settings to study stereochemical effects in organic reactions and to develop new synthetic methodologies.

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