Methyl (S)-4-Benzyl-5-oxomorpholine-3-carboxylate

≥97%

Reagent Code: #57169
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CAS Number 1235181-00-6

science Other reagents with same CAS 1235181-00-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.26 g/mol
Formula C₁₃H₁₅NO₄
badge Registry Numbers
MDL Number MFCD11501467
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the production of various bioactive molecules, including those with potential therapeutic applications. Its structural features make it valuable for constructing complex morpholine derivatives, which are often explored for their pharmacological properties, such as enzyme inhibition or receptor modulation. Additionally, it is employed in research settings to study stereochemistry and reaction mechanisms due to its chiral center. Its role in medicinal chemistry is significant, as it contributes to the synthesis of drug candidates targeting diseases like cancer, infections, or neurological disorders.

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Test Parameter Specification
Appearance White to Yellow solid
Purity 97-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿585.00
inventory 1g
10-20 days ฿1,880.00
inventory 5g
10-20 days ฿6,700.00

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Methyl (S)-4-Benzyl-5-oxomorpholine-3-carboxylate
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This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the production of various bioactive molecules, including those with potential therapeutic applications. Its structural features make it valuable for constructing complex morpholine derivatives, which are often explored for their pharmacological properties, such as enzyme inhibition or receptor modulation. Additionally, it is employed in research settings to study stereochemistry and reaction mechanisms due to its chiral center. Its role in medicinal chemistry is significant, as it contributes to the synthesis of drug candidates targeting diseases like cancer, infections, or neurological disorders.
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