7-(Trifluoromethyl)-1H-indazole

95%

Reagent Code: #240878
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CAS Number 885694-00-8

science Other reagents with same CAS 885694-00-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.13 g/mol
Formula C₈H₅F₃N₂
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Shows utility in medicinal chemistry for designing drugs targeting inflammatory diseases and neurodegenerative disorders due to its ability to modulate enzyme activity. Also employed in agrochemical research for creating novel pesticides with improved stability and efficacy. Its trifluoromethyl group enhances metabolic resistance and lipophilicity, making it valuable in optimizing drug candidates for better bioavailability and target binding.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿920.00
100mg
10-20 days ฿2,200.00
250mg
10-20 days ฿3,040.00
1g
10-20 days ฿9,840.00
5g
10-20 days ฿36,740.00
7-(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. Shows utility in medicinal chemistry for designing drugs targeting inflammatory diseases and neurodegenerative disorders due to its ability to modulate enzyme activity. Also employed in agrochemical research for creating novel pesticides with improved stability and efficacy. Its trifluoromethyl group enhances metabolic resistance and lipophilicity, making it

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Shows utility in medicinal chemistry for designing drugs targeting inflammatory diseases and neurodegenerative disorders due to its ability to modulate enzyme activity. Also employed in agrochemical research for creating novel pesticides with improved stability and efficacy. Its trifluoromethyl group enhances metabolic resistance and lipophilicity, making it valuable in optimizing drug candidates for better bioavailability and target binding.

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