ethyl(S)-3-amino-3-(pyridin-3-yl)propanoate

Reagent Code: #51366
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CAS Number 149519-95-9

science Other reagents with same CAS 149519-95-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.23 g/mol
Formula C₁₀H₁₄N₂O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It is particularly valuable in the development of drugs targeting neurological disorders, such as Alzheimer's disease and Parkinson's disease, due to its structural compatibility with neurotransmitter analogs. Additionally, it finds application in the production of chiral compounds, leveraging its stereochemistry to create enantiomerically pure substances critical for therapeutic efficacy. Its pyridine moiety also makes it a useful building block in designing molecules with potential anti-inflammatory and anticancer properties.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00
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ethyl(S)-3-amino-3-(pyridin-3-yl)propanoate
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It is particularly valuable in the development of drugs targeting neurological disorders, such as Alzheimer's disease and Parkinson's disease, due to its structural compatibility with neurotransmitter analogs. Additionally, it finds application in the production of chiral compounds, leveraging its stereochemistry to create enantiomerically pure substa

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It is particularly valuable in the development of drugs targeting neurological disorders, such as Alzheimer's disease and Parkinson's disease, due to its structural compatibility with neurotransmitter analogs. Additionally, it finds application in the production of chiral compounds, leveraging its stereochemistry to create enantiomerically pure substances critical for therapeutic efficacy. Its pyridine moiety also makes it a useful building block in designing molecules with potential anti-inflammatory and anticancer properties.

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