5,7-Dichloro-2-((dimethylamino)methyl)quinolin-8-ol

98%

Reagent Code: #178748
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CAS Number 747408-78-2

science Other reagents with same CAS 747408-78-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.14 g/mol
Formula C₁₂H₁₂Cl₂N₂O
badge Registry Numbers
MDL Number MFCD30749371
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily in the synthesis of pharmaceutical intermediates, this compound serves as a key building block in the development of kinase inhibitors, particularly for targeted cancer therapies. Its structure allows for selective binding to certain enzyme active sites, making it valuable in the design of drugs that modulate cellular signaling pathways. It is also employed in research settings to develop novel compounds with potential antiviral and anti-inflammatory properties. Due to its amine functionality and aromatic scaffold, it participates in various coupling and functionalization reactions, supporting its use in medicinal chemistry and drug discovery programs.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,070.00
inventory 250mg
10-20 days ฿32,500.00
inventory 10mg
10-20 days ฿3,470.00

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5,7-Dichloro-2-((dimethylamino)methyl)quinolin-8-ol
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Used primarily in the synthesis of pharmaceutical intermediates, this compound serves as a key building block in the development of kinase inhibitors, particularly for targeted cancer therapies. Its structure allows for selective binding to certain enzyme active sites, making it valuable in the design of drugs that modulate cellular signaling pathways. It is also employed in research settings to develop novel compounds with potential antiviral and anti-inflammatory properties. Due to its amine functional

Used primarily in the synthesis of pharmaceutical intermediates, this compound serves as a key building block in the development of kinase inhibitors, particularly for targeted cancer therapies. Its structure allows for selective binding to certain enzyme active sites, making it valuable in the design of drugs that modulate cellular signaling pathways. It is also employed in research settings to develop novel compounds with potential antiviral and anti-inflammatory properties. Due to its amine functionality and aromatic scaffold, it participates in various coupling and functionalization reactions, supporting its use in medicinal chemistry and drug discovery programs.

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