Methyl (R)-3-amino-3-(pyridin-3-yl)propanoate dihydrochloride

95%

Reagent Code: #229408
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CAS Number 1016558-17-0

science Other reagents with same CAS 1016558-17-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.13 g/mol
Formula C₉H₁₄Cl₂N₂O₂
badge Registry Numbers
MDL Number MFCD11111366
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of serotonin-norepinephrine reuptake inhibitors (SNRIs) like duloxetine. Its chiral amine structure enables selective biological activity, making it valuable in developing drugs for treating depression, anxiety, and neuropathic pain. The pyridine ring enhances binding affinity to target receptors, while the ester group allows for further chemical modifications during drug development. Commonly employed in asymmetric synthesis routes due to its enantiomeric purity, ensuring high efficacy and reduced side effects in final drug products.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,050.00
inventory 250mg
10-20 days ฿33,200.00

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Methyl (R)-3-amino-3-(pyridin-3-yl)propanoate dihydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of serotonin-norepinephrine reuptake inhibitors (SNRIs) like duloxetine. Its chiral amine structure enables selective biological activity, making it valuable in developing drugs for treating depression, anxiety, and neuropathic pain. The pyridine ring enhances binding affinity to target receptors, while the ester group allows for further chemical modifications during drug development. Commonly employed in asymm

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of serotonin-norepinephrine reuptake inhibitors (SNRIs) like duloxetine. Its chiral amine structure enables selective biological activity, making it valuable in developing drugs for treating depression, anxiety, and neuropathic pain. The pyridine ring enhances binding affinity to target receptors, while the ester group allows for further chemical modifications during drug development. Commonly employed in asymmetric synthesis routes due to its enantiomeric purity, ensuring high efficacy and reduced side effects in final drug products.

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