1-(5-bromo-3-(trifluoromethyl)pyridin-2-yl)hydrazine

≥95%

Reagent Code: #144080
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CAS Number 1374652-48-8

science Other reagents with same CAS 1374652-48-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.02 g/mol
Formula C₆H₅BrF₃N₃
badge Registry Numbers
MDL Number MFCD22375529
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrazone derivatives with carbonyl compounds, enabling the creation of biologically active molecules. Also employed in agrochemical research for designing new pesticides with improved efficacy and selectivity. Its bromo and trifluoromethyl groups facilitate further functionalization through cross-coupling reactions, making it valuable in structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,560.00
inventory 1g
10-20 days ฿12,120.00
inventory 5g
10-20 days ฿44,570.00
inventory 10g
10-20 days ฿77,500.00
inventory 100mg
10-20 days ฿3,580.00

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1-(5-bromo-3-(trifluoromethyl)pyridin-2-yl)hydrazine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrazone derivatives with carbonyl compounds, enabling the creation of biologically active molecules. Also employed in agrochemical research for designing new pesticides with improved efficacy and selectivity. Its bromo and trifluoromethyl groups facilitate further functionalization

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrazone derivatives with carbonyl compounds, enabling the creation of biologically active molecules. Also employed in agrochemical research for designing new pesticides with improved efficacy and selectivity. Its bromo and trifluoromethyl groups facilitate further functionalization through cross-coupling reactions, making it valuable in structure-activity relationship studies.

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