(S)-Methyl 2-amino-3-(3-methoxyphenyl)propanoate hydrochloride

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Reagent Code: #236231
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CAS Number 72747-20-7

science Other reagents with same CAS 72747-20-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.70 g/mol
Formula C₁₁H₁₆ClNO₃
badge Registry Numbers
MDL Number MFCD12911140
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of serotonin-norepinephrine reuptake inhibitors (SNRIs) like duloxetine. Its enantiomeric purity is critical for achieving the desired biological activity in the final drug substance. Commonly employed in asymmetric synthesis routes where the ester functionality allows for further chemical modifications, such as hydrolysis or coupling reactions. Also utilized in the development of active pharmaceutical ingredients (APIs) requiring a phenylpropanamine backbone with specific stereochemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,940.00
inventory 250mg
10-20 days ฿11,860.00
inventory 1g
10-20 days ฿34,060.00

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(S)-Methyl 2-amino-3-(3-methoxyphenyl)propanoate hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of serotonin-norepinephrine reuptake inhibitors (SNRIs) like duloxetine. Its enantiomeric purity is critical for achieving the desired biological activity in the final drug substance. Commonly employed in asymmetric synthesis routes where the ester functionality allows for further chemical modifications, such as hydrolysis or coupling reactions. Also utilized in the development of active pharmaceutical i

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of serotonin-norepinephrine reuptake inhibitors (SNRIs) like duloxetine. Its enantiomeric purity is critical for achieving the desired biological activity in the final drug substance. Commonly employed in asymmetric synthesis routes where the ester functionality allows for further chemical modifications, such as hydrolysis or coupling reactions. Also utilized in the development of active pharmaceutical ingredients (APIs) requiring a phenylpropanamine backbone with specific stereochemistry.

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