(2R,3S)-4-(tert-Butoxycarbonyl)-2-methylmorpholine-3-carboxylic acid

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Reagent Code: #55340
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CAS Number 1807938-50-6

science Other reagents with same CAS 1807938-50-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.2723 g/mol
Formula C₁₁H₁₉NO₅
badge Registry Numbers
MDL Number MFCD22394660
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules. Its structure, featuring a morpholine ring and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in the development of active pharmaceutical ingredients (APIs). The Boc group is particularly useful in peptide synthesis, where it protects amines during reactions and can be easily removed under acidic conditions. Additionally, the stereochemistry of the compound allows it to be employed in the production of chiral drugs, where specific enantiomers are required for therapeutic efficacy. Its carboxylic acid functionality also enables further chemical modifications, making it a versatile building block in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,636.00

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(2R,3S)-4-(tert-Butoxycarbonyl)-2-methylmorpholine-3-carboxylic acid
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This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules. Its structure, featuring a morpholine ring and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in the development of active pharmaceutical ingredients (APIs). The Boc group is particularly useful in peptide synthesis, where it protects amines during reactions and can be easily removed under acidic conditions. Additionally, the stereochemistry of the compound al

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules. Its structure, featuring a morpholine ring and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in the development of active pharmaceutical ingredients (APIs). The Boc group is particularly useful in peptide synthesis, where it protects amines during reactions and can be easily removed under acidic conditions. Additionally, the stereochemistry of the compound allows it to be employed in the production of chiral drugs, where specific enantiomers are required for therapeutic efficacy. Its carboxylic acid functionality also enables further chemical modifications, making it a versatile building block in medicinal chemistry.

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