(R)-4-tert-Butyl 3-methyl morpholine-3,4-dicarboxylate

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Reagent Code: #71266
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CAS Number 885321-46-0

science Other reagents with same CAS 885321-46-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.27 g/mol
Formula C₁₁H₁₉NO₅
badge Registry Numbers
MDL Number MFCD09953091
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the pharmaceutical and chemical research industries as a chiral building block. Its stereospecific structure makes it valuable in the synthesis of enantiomerically pure drugs, particularly in the development of active pharmaceutical ingredients (APIs) where chirality plays a critical role in efficacy and safety. It is also employed in the preparation of complex organic molecules, serving as an intermediate in multi-step synthetic processes. Additionally, its application extends to asymmetric catalysis, where it aids in the production of optically active compounds with high selectivity. Researchers leverage its unique morpholine core to design and develop novel compounds with potential therapeutic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,129.00
inventory 100mg
10-20 days ฿3,843.00
inventory 1g
10-20 days ฿15,363.00

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(R)-4-tert-Butyl 3-methyl morpholine-3,4-dicarboxylate
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This compound is primarily utilized in the pharmaceutical and chemical research industries as a chiral building block. Its stereospecific structure makes it valuable in the synthesis of enantiomerically pure drugs, particularly in the development of active pharmaceutical ingredients (APIs) where chirality plays a critical role in efficacy and safety. It is also employed in the preparation of complex organic molecules, serving as an intermediate in multi-step synthetic processes. Additionally, its applica

This compound is primarily utilized in the pharmaceutical and chemical research industries as a chiral building block. Its stereospecific structure makes it valuable in the synthesis of enantiomerically pure drugs, particularly in the development of active pharmaceutical ingredients (APIs) where chirality plays a critical role in efficacy and safety. It is also employed in the preparation of complex organic molecules, serving as an intermediate in multi-step synthetic processes. Additionally, its application extends to asymmetric catalysis, where it aids in the production of optically active compounds with high selectivity. Researchers leverage its unique morpholine core to design and develop novel compounds with potential therapeutic properties.

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