(S)-3-Methylmorpholine

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Reagent Code: #234747
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CAS Number 350595-57-2

science Other reagents with same CAS 350595-57-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 101.15 g/mol
Formula C₅H₁₁NO
badge Registry Numbers
MDL Number MFCD03840369
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a chiral building block in pharmaceutical synthesis, particularly in the production of active pharmaceutical ingredients where stereochemistry is critical. It serves as an intermediate in the development of drugs targeting central nervous system disorders and anti-inflammatory agents. Its structural configuration allows for selective interactions with biological targets, enhancing drug efficacy and reducing side effects. Also employed in the preparation of catalysts for asymmetric synthesis, supporting the creation of enantiomerically pure compounds in research and industrial settings.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿300.00
inventory 1g
10-20 days ฿380.00
inventory 25g
10-20 days ฿5,680.00
inventory 100g
10-20 days ฿22,650.00
inventory 5g
10-20 days ฿1,450.00
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(S)-3-Methylmorpholine
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Used as a chiral building block in pharmaceutical synthesis, particularly in the production of active pharmaceutical ingredients where stereochemistry is critical. It serves as an intermediate in the development of drugs targeting central nervous system disorders and anti-inflammatory agents. Its structural configuration allows for selective interactions with biological targets, enhancing drug efficacy and reducing side effects. Also employed in the preparation of catalysts for asymmetric synthesis, supp

Used as a chiral building block in pharmaceutical synthesis, particularly in the production of active pharmaceutical ingredients where stereochemistry is critical. It serves as an intermediate in the development of drugs targeting central nervous system disorders and anti-inflammatory agents. Its structural configuration allows for selective interactions with biological targets, enhancing drug efficacy and reducing side effects. Also employed in the preparation of catalysts for asymmetric synthesis, supporting the creation of enantiomerically pure compounds in research and industrial settings.

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