(S)-2-Amino-3-(5-chloropyridin-2-yl)propanoic acid dihydrochloride

95%

Reagent Code: #233466
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CAS Number 2703746-01-2

science Other reagents with same CAS 2703746-01-2

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Weight 273.54 g/mol
Formula C₈H₁₁Cl₃N₂O₂
badge Registry Numbers
MDL Number MFCD34186981
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of neuroactive compounds targeting glutamate receptors. Its structural configuration supports the creation of analogs with modulatory effects on central nervous system activity. Commonly employed in research settings for designing drugs related to cognitive disorders and neurological diseases. Also utilized in medicinal chemistry for structure-activity relationship studies due to its chiral stability and functional group compatibility.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,050.00
inventory 250mg
10-20 days ฿33,020.00

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(S)-2-Amino-3-(5-chloropyridin-2-yl)propanoic acid dihydrochloride
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of neuroactive compounds targeting glutamate receptors. Its structural configuration supports the creation of analogs with modulatory effects on central nervous system activity. Commonly employed in research settings for designing drugs related to cognitive disorders and neurological diseases. Also utilized in medicinal chemistry for structure-activity relationship studies due to its chiral stability and fu
Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of neuroactive compounds targeting glutamate receptors. Its structural configuration supports the creation of analogs with modulatory effects on central nervous system activity. Commonly employed in research settings for designing drugs related to cognitive disorders and neurological diseases. Also utilized in medicinal chemistry for structure-activity relationship studies due to its chiral stability and functional group compatibility.
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