4-Bromo-1-(2-methoxyethyl)-3,5-dimethyl-1H-pyrazole

95%

Reagent Code: #140973
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CAS Number 1342761-60-7

science Other reagents with same CAS 1342761-60-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.1 g/mol
Formula C₈H₁₃N₂OBr
badge Registry Numbers
MDL Number MFCD16687003
thermostat Physical Properties
Boiling Point 279.7±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.41±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of pyrazole-based bioactive compounds. Its structure supports the creation of derivatives with insecticidal, fungicidal, or anti-inflammatory properties. The bromo and ether functionalities allow for further chemical modifications through cross-coupling reactions or nucleophilic substitutions, making it valuable in medicinal chemistry and crop protection research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,340.00
inventory 1g
10-20 days ฿29,030.00

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4-Bromo-1-(2-methoxyethyl)-3,5-dimethyl-1H-pyrazole
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of pyrazole-based bioactive compounds. Its structure supports the creation of derivatives with insecticidal, fungicidal, or anti-inflammatory properties. The bromo and ether functionalities allow for further chemical modifications through cross-coupling reactions or nucleophilic substitutions, making it valuable in medicinal chemistry and crop protection research.

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of pyrazole-based bioactive compounds. Its structure supports the creation of derivatives with insecticidal, fungicidal, or anti-inflammatory properties. The bromo and ether functionalities allow for further chemical modifications through cross-coupling reactions or nucleophilic substitutions, making it valuable in medicinal chemistry and crop protection research.

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