4-Bromo-3,5-dimethyl-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazole

97%

Reagent Code: #152333
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CAS Number 1339665-24-5

science Other reagents with same CAS 1339665-24-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.14 g/mol
Formula C₁₀H₁₅BrN₂O
badge Registry Numbers
MDL Number MFCD19611978
thermostat Physical Properties
Boiling Point 346.9±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.53±0.1 g/cm3(Predicted)
Storage Room temperature, sealed

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other therapeutic agents targeting inflammatory diseases and cancer. Its structure allows for selective modifications, making it valuable in structure-activity relationship (SAR) studies. Commonly employed in cross-coupling reactions to introduce aryl or heteroaryl groups, enhancing molecular diversity in drug discovery programs. Also utilized in agrochemical research for designing new pesticides with improved efficacy and selectivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿6,680.00
250mg
10-20 days ฿11,330.00
1g
10-20 days ฿30,530.00
4-Bromo-3,5-dimethyl-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazole
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other therapeutic agents targeting inflammatory diseases and cancer. Its structure allows for selective modifications, making it valuable in structure-activity relationship (SAR) studies. Commonly employed in cross-coupling reactions to introduce aryl or heteroaryl groups, enhancing molecular diversity in drug discovery p

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other therapeutic agents targeting inflammatory diseases and cancer. Its structure allows for selective modifications, making it valuable in structure-activity relationship (SAR) studies. Commonly employed in cross-coupling reactions to introduce aryl or heteroaryl groups, enhancing molecular diversity in drug discovery programs. Also utilized in agrochemical research for designing new pesticides with improved efficacy and selectivity.

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