Methyl (S)-3-amino-3-(3-chlorophenyl)propanoate hydrochloride

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Reagent Code: #202868
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CAS Number 1245606-65-8

science Other reagents with same CAS 1245606-65-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.12 g/mol
Formula C₁₀H₁₃Cl₂NO₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of serotonin-norepinephrine reuptake inhibitors (SNRIs) for treating depression and anxiety disorders. Its enantiomerically pure structure enables selective biological activity, improving drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis routes where the ester functionality allows for further chemical modifications, such as hydrolysis or amidation, to build complex active pharmaceutical ingredients (APIs). Also utilized in research settings for developing novel CNS-targeting compounds due to its ability to cross the blood-brain barrier effectively.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,750.00
inventory 1g
10-20 days ฿72,160.00

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Methyl (S)-3-amino-3-(3-chlorophenyl)propanoate hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of serotonin-norepinephrine reuptake inhibitors (SNRIs) for treating depression and anxiety disorders. Its enantiomerically pure structure enables selective biological activity, improving drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis routes where the ester functionality allows for further chemical modifications, such as hydrolysis or amidation, to build complex

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of serotonin-norepinephrine reuptake inhibitors (SNRIs) for treating depression and anxiety disorders. Its enantiomerically pure structure enables selective biological activity, improving drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis routes where the ester functionality allows for further chemical modifications, such as hydrolysis or amidation, to build complex active pharmaceutical ingredients (APIs). Also utilized in research settings for developing novel CNS-targeting compounds due to its ability to cross the blood-brain barrier effectively.

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