(S)-2-Acetamido-3-(4-hydroxyphenyl)-N-methylpropanamide

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Reagent Code: #233290
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CAS Number 6367-14-2

science Other reagents with same CAS 6367-14-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.27 g/mol
Formula C₁₂H₁₆N₂O₃
badge Registry Numbers
MDL Number MFCD00237518
thermostat Physical Properties
Melting Point 192.2-193.3 °C
Boiling Point 593.2±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.187±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its chiral structure and functional groups make it valuable in asymmetric synthesis for creating enantiomerically pure drugs. Commonly employed in research settings for designing enzyme inhibitors, especially targeting serine proteases. Also utilized in the preparation of peptide mimetics due to its structural similarity to natural amino acid derivatives.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,340.00
inventory 1g
10-20 days ฿30,190.00

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(S)-2-Acetamido-3-(4-hydroxyphenyl)-N-methylpropanamide
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its chiral structure and functional groups make it valuable in asymmetric synthesis for creating enantiomerically pure drugs. Commonly employed in research settings for designing enzyme inhibitors, especially targeting serine proteases. Also utilized in the preparation of peptide mimetics due to its structural similarity to natural amino acid derivatives.

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its chiral structure and functional groups make it valuable in asymmetric synthesis for creating enantiomerically pure drugs. Commonly employed in research settings for designing enzyme inhibitors, especially targeting serine proteases. Also utilized in the preparation of peptide mimetics due to its structural similarity to natural amino acid derivatives.

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