7-Bromo-5-(trifluoromethyl)-1H-indazole

98%

Reagent Code: #148368
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CAS Number 1100212-66-5

science Other reagents with same CAS 1100212-66-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.03 g/mol
Formula C₈H₄BrF₃N₂
badge Registry Numbers
MDL Number MFCD27939136
thermostat Physical Properties
Boiling Point 309.2±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

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, making it valuable in drug discovery for targeting specific signaling pathways. Also employed in the creation of agrochemicals due to its stability and reactivity in forming complex heterocyclic systems. Commonly utilized in research settings to build more complex molecules through cross-coupling reactions and nucleophilic substitutions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,600.00
inventory 1g
10-20 days ฿6,180.00

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7-Bromo-5-(trifluoromethyl)-1H-indazole
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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, making it valuable in drug discovery for targeting specific signaling pathways. Also employed in the creation of agrochemicals due to its stability and reactivity in forming complex heterocyclic systems. Commonly utilized in research settings to build more complex molecules through cross-coupling reaction

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, making it valuable in drug discovery for targeting specific signaling pathways. Also employed in the creation of agrochemicals due to its stability and reactivity in forming complex heterocyclic systems. Commonly utilized in research settings to build more complex molecules through cross-coupling reactions and nucleophilic substitutions.

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