4-Bromo-8-(trifluoromethyl)quinoline

≥95%

Reagent Code: #119368
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CAS Number 260973-10-2

science Other reagents with same CAS 260973-10-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.05 g/mol
Formula C₁₀H₅BrF₃N
badge Registry Numbers
MDL Number MFCD08063211
thermostat Physical Properties
Boiling Point 301.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the creation of potential drug candidates targeting infectious diseases, due to the presence of both bromine and trifluoromethyl groups, which enhance binding affinity and metabolic stability. Additionally, it is utilized in material science for the development of organic electronic materials, where its quinoline core contributes to desirable electronic properties. In agrochemical research, it is explored for the design of novel pesticides and herbicides, leveraging its unique chemical framework to improve efficacy and selectivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿4,914.00
250mg
10-20 days ฿1,665.00
100mg
10-20 days ฿972.00
5g
10-20 days ฿23,220.00
4-Bromo-8-(trifluoromethyl)quinoline
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Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the creation of potential drug candidates targeting infectious diseases, due to the presence of both bromine and trifluoromethyl groups, which enhance binding affinity and metabolic stability. Additionally, it is utilized in material science for the development of organic electronic materials, where its q

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the creation of potential drug candidates targeting infectious diseases, due to the presence of both bromine and trifluoromethyl groups, which enhance binding affinity and metabolic stability. Additionally, it is utilized in material science for the development of organic electronic materials, where its quinoline core contributes to desirable electronic properties. In agrochemical research, it is explored for the design of novel pesticides and herbicides, leveraging its unique chemical framework to improve efficacy and selectivity.

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