(R)-2-Amino-2-(pyridin-2-yl)ethanol dihydrochloride

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Reagent Code: #231299
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CAS Number 2097958-04-6

science Other reagents with same CAS 2097958-04-6

blur_circular Chemical Specifications

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Weight 211.09 g/mol
Formula C₇H₁₂Cl₂N₂O
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in pharmaceutical synthesis, particularly as a chiral building block for drugs targeting central nervous system disorders. Its structural motif is valuable in developing enzyme inhibitors and receptor modulators. Commonly employed in the preparation of bioactive molecules due to the presence of both amino and hydroxyl functional groups in a stereochemically defined arrangement. Also utilized in asymmetric synthesis and catalysis as a ligand precursor. Its pyridine-containing scaffold supports binding interactions in medicinal chemistry applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,280.00
inventory 250mg
10-20 days ฿6,370.00
inventory 1g
10-20 days ฿18,950.00
inventory 5g
10-20 days ฿82,350.00

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(R)-2-Amino-2-(pyridin-2-yl)ethanol dihydrochloride
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Used in pharmaceutical synthesis, particularly as a chiral building block for drugs targeting central nervous system disorders. Its structural motif is valuable in developing enzyme inhibitors and receptor modulators. Commonly employed in the preparation of bioactive molecules due to the presence of both amino and hydroxyl functional groups in a stereochemically defined arrangement. Also utilized in asymmetric synthesis and catalysis as a ligand precursor. Its pyridine-containing scaffold supports binding i
Used in pharmaceutical synthesis, particularly as a chiral building block for drugs targeting central nervous system disorders. Its structural motif is valuable in developing enzyme inhibitors and receptor modulators. Commonly employed in the preparation of bioactive molecules due to the presence of both amino and hydroxyl functional groups in a stereochemically defined arrangement. Also utilized in asymmetric synthesis and catalysis as a ligand precursor. Its pyridine-containing scaffold supports binding interactions in medicinal chemistry applications.
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