(R)-2-Amino-N-benzyl-3-methoxypropanamide

95%

Reagent Code: #85790
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CAS Number 196601-69-1

science Other reagents with same CAS 196601-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.26 g/mol
Formula C₁₁H₁₆N₂O₂
badge Registry Numbers
MDL Number MFCD14708219
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, dry, sealed

description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various bioactive molecules. Its chiral structure makes it valuable in the development of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular disorders. The presence of the benzyl and methoxy groups enhances its ability to interact with specific biological receptors, making it a key component in the design of receptor modulators and enzyme inhibitors. Additionally, it is employed in research settings to study the structure-activity relationships of compounds with similar scaffolds, aiding in the discovery of new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,926.00
inventory 250mg
10-20 days ฿3,276.00
inventory 1g
10-20 days ฿8,514.00

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(R)-2-Amino-N-benzyl-3-methoxypropanamide
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This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various bioactive molecules. Its chiral structure makes it valuable in the development of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular disorders. The presence of the benzyl and methoxy groups enhances its ability to interact with specific biological receptors, making it a key component in the design of receptor modulators and enzyme inhibitors. Additionall

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various bioactive molecules. Its chiral structure makes it valuable in the development of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular disorders. The presence of the benzyl and methoxy groups enhances its ability to interact with specific biological receptors, making it a key component in the design of receptor modulators and enzyme inhibitors. Additionally, it is employed in research settings to study the structure-activity relationships of compounds with similar scaffolds, aiding in the discovery of new therapeutic agents.

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