3-Bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole

95%

Reagent Code: #150250
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CAS Number 1044270-96-3

science Other reagents with same CAS 1044270-96-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.09 g/mol
Formula C₈H₁₁BrN₂O
badge Registry Numbers
MDL Number MFCD16659986
thermostat Physical Properties
Boiling Point 328.5±32.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce pyrazole motifs into drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,140.00
inventory 250mg
10-20 days ฿1,780.00
inventory 1g
10-20 days ฿2,790.00
inventory 5g
10-20 days ฿12,180.00
inventory 25g
10-20 days ฿51,180.00

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3-Bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce pyrazole motifs into drug candidates. Also utilized in agrochemical research for designing novel p

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce pyrazole motifs into drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its stability and reactivity profile.

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