5-Bromo-1-methyl-1H-pyrazol-4-amine

95%

Reagent Code: #141112
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CAS Number 1504254-19-6

science Other reagents with same CAS 1504254-19-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.01 g/mol
Formula C₄H₆BrN₃
badge Registry Numbers
MDL Number MFCD26679038
thermostat Physical Properties
Boiling Point 274.6±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.91±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals and bioactive molecules due to its ability to form stable heterocyclic structures. Its bromo and amine functional groups allow for easy modification through cross-coupling and substitution reactions, making it valuable in medicinal chemistry research and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,260.00
inventory 250mg
10-20 days ฿19,140.00
inventory 1g
10-20 days ฿51,670.00

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5-Bromo-1-methyl-1H-pyrazol-4-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals and bioactive molecules due to its ability to form stable heterocyclic structures. Its bromo and amine functional groups allow for easy modification through cross-coupling and substitution reactions, making it valuable in medicinal chemistry research and drug discovery.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals and bioactive molecules due to its ability to form stable heterocyclic structures. Its bromo and amine functional groups allow for easy modification through cross-coupling and substitution reactions, making it valuable in medicinal chemistry research and drug discovery.

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