8-BROMO-2-(TRIFLUOROMETHYL)QUINOLIN-4-OL

95%

Reagent Code: #144706
label
Alias 2-Trifluoromethyl-4-hydroxy-8-bromoquinoline
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CAS Number 59108-43-9

science Other reagents with same CAS 59108-43-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.05 g/mol
Formula C₁₀H₅BrF₃NO
thermostat Physical Properties
Melting Point 136 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing selectivity and potency. Also employed in the preparation of fluorinated quinoline derivatives with antimicrobial and anti-inflammatory properties. Commonly utilized in medicinal chemistry research for structure-activity relationship (SAR) studies due to its halogen and trifluoromethyl functional groups, which influence metabolic stability and lipophilicity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,110.00
inventory 5g
10-20 days ฿2,964.00

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8-BROMO-2-(TRIFLUOROMETHYL)QUINOLIN-4-OL
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing selectivity and potency. Also employed in the preparation of fluorinated quinoline derivatives with antimicrobial and anti-inflammatory properties. Commonly utilized in medicinal chemistry research for structure-activity relationship (SAR) studies due to its halogen and trifluoromethyl functiona

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing selectivity and potency. Also employed in the preparation of fluorinated quinoline derivatives with antimicrobial and anti-inflammatory properties. Commonly utilized in medicinal chemistry research for structure-activity relationship (SAR) studies due to its halogen and trifluoromethyl functional groups, which influence metabolic stability and lipophilicity.

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