4-Bromo-5-methyl-3-nitro-1H-pyrazole

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Reagent Code: #47492
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CAS Number 70951-96-1

science Other reagents with same CAS 70951-96-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.00 g/mol
Formula C₄H₄BrN₃O₂
badge Registry Numbers
MDL Number MFCD00195045
thermostat Physical Properties
Boiling Point 331.9±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its reactive sites, including the bromo, nitro, and methyl groups, make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create diverse heterocyclic compounds. Additionally, its nitro group can be reduced to form amines, which are essential in the production of various bioactive molecules. The compound’s structural features also make it suitable for studying structure-activity relationships in drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿774.00
inventory 5g
10-20 days ฿9,198.00
inventory 250mg
10-20 days ฿1,215.00
inventory 1g
10-20 days ฿3,060.00

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4-Bromo-5-methyl-3-nitro-1H-pyrazole
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This compound is primarily utilized in the field of organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its reactive sites, including the bromo, nitro, and methyl groups, make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create diverse heterocyclic compounds. Additionally, its nitro group can be reduc

This compound is primarily utilized in the field of organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its reactive sites, including the bromo, nitro, and methyl groups, make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create diverse heterocyclic compounds. Additionally, its nitro group can be reduced to form amines, which are essential in the production of various bioactive molecules. The compound’s structural features also make it suitable for studying structure-activity relationships in drug discovery.

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