(R)-2-Amino-2-(3,5-difluoropyridin-2-yl)ethanol dihydrochloride

97%

Reagent Code: #229330
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CAS Number 2828431-90-7

science Other reagents with same CAS 2828431-90-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.07 g/mol
Formula C₇H₁₀Cl₂F₂N₂O
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of biologically active pharmaceuticals, particularly in the development of kinase inhibitors. Its structural features allow for selective interactions with enzyme targets, making it valuable in the production of drugs for cancer and inflammatory diseases. The compound's stereochemistry enhances binding affinity and specificity, improving drug efficacy and reducing off-target effects. Commonly employed in late-stage functionalization due to its stability and reactivity profile under various coupling conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,440.00
inventory 250mg
10-20 days ฿36,420.00

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(R)-2-Amino-2-(3,5-difluoropyridin-2-yl)ethanol dihydrochloride
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Used as a key chiral intermediate in the synthesis of biologically active pharmaceuticals, particularly in the development of kinase inhibitors. Its structural features allow for selective interactions with enzyme targets, making it valuable in the production of drugs for cancer and inflammatory diseases. The compound's stereochemistry enhances binding affinity and specificity, improving drug efficacy and reducing off-target effects. Commonly employed in late-stage functionalization due to its stability

Used as a key chiral intermediate in the synthesis of biologically active pharmaceuticals, particularly in the development of kinase inhibitors. Its structural features allow for selective interactions with enzyme targets, making it valuable in the production of drugs for cancer and inflammatory diseases. The compound's stereochemistry enhances binding affinity and specificity, improving drug efficacy and reducing off-target effects. Commonly employed in late-stage functionalization due to its stability and reactivity profile under various coupling conditions.

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