(r)-(4-Benzyl-morpholin-3-yl)-aceticacidmethylester

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Reagent Code: #156035
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CAS Number 917572-30-6

science Other reagents with same CAS 917572-30-6

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scatter_plot Molecular Information
Weight 249.31 g/mol
Formula C₁₄H₁₉NO₃
badge Registry Numbers
MDL Number MFCD10687129
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its chiral structure makes it valuable in producing enantiomerically pure compounds, which are critical for targeted biological activity. Commonly employed in the preparation of neurokinin antagonists and other neuromodulatory therapeutics. Also utilized in research settings for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and blood-brain barrier penetration in drug candidates.

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inventory 1g
10-20 days ฿93,450.00

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(r)-(4-Benzyl-morpholin-3-yl)-aceticacidmethylester
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its chiral structure makes it valuable in producing enantiomerically pure compounds, which are critical for targeted biological activity. Commonly employed in the preparation of neurokinin antagonists and other neuromodulatory therapeutics. Also utilized in research settings for structure-activity relationship (SAR) studies due to its ability to enhance metabolic st

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its chiral structure makes it valuable in producing enantiomerically pure compounds, which are critical for targeted biological activity. Commonly employed in the preparation of neurokinin antagonists and other neuromodulatory therapeutics. Also utilized in research settings for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and blood-brain barrier penetration in drug candidates.

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