(R)-1-(2-Methoxypyridin-4-yl)ethanamine

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Reagent Code: #231056
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CAS Number 1213559-80-8

science Other reagents with same CAS 1213559-80-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.196 g/mol
Formula C₈H₁₂N₂O
badge Registry Numbers
MDL Number MFCD11859028
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structural features allow for selective binding to specific enzyme active sites, enhancing drug efficacy and reducing off-target effects. Commonly employed in the preparation of investigational oncology compounds due to its metabolic stability and favorable pharmacokinetic profile. Also utilized in asymmetric synthesis to introduce chirality in active pharmaceutical ingredients (APIs), improving enantiomeric purity and biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,400.00
inventory 250mg
10-20 days ฿21,880.00
inventory 1g
10-20 days ฿61,120.00
(R)-1-(2-Methoxypyridin-4-yl)ethanamine
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structural features allow for selective binding to specific enzyme active sites, enhancing drug efficacy and reducing off-target effects. Commonly employed in the preparation of investigational oncology compounds due to its metabolic stability and favorable pharmacokinetic profile. Also utilized in asymmetric synthesis to introduce chirality

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structural features allow for selective binding to specific enzyme active sites, enhancing drug efficacy and reducing off-target effects. Commonly employed in the preparation of investigational oncology compounds due to its metabolic stability and favorable pharmacokinetic profile. Also utilized in asymmetric synthesis to introduce chirality in active pharmaceutical ingredients (APIs), improving enantiomeric purity and biological activity.

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