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

95%

Reagent Code: #151342
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CAS Number 1248908-53-3

science Other reagents with same CAS 1248908-53-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.24 g/mol
Formula C₁₁H₁₃N₃
badge Registry Numbers
MDL Number MFCD16042721
thermostat Physical Properties
Boiling Point 370.7±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.14±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in π-π stacking interactions, enhancing binding affinity to target proteins. Also utilized in the preparation of agrochemicals and dyes, where its structural features contribute to improved stability and biological activity. Its amine functionality allows for easy derivatization, making it valuable in combinatorial chemistry and high-throughput screening for drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,580.00
inventory 100mg
10-20 days ฿10,610.00
inventory 250mg
10-20 days ฿14,860.00
inventory 1g
10-20 days ฿38,650.00

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1-Benzyl-5-methyl-1H-pyrazol-4-amine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in π-π stacking interactions, enhancing binding affinity to target proteins. Also utilized in the preparation of agrochemicals and dyes, where its structural features contribute to improved stability and biological activity. Its amine functionality allows fo

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in π-π stacking interactions, enhancing binding affinity to target proteins. Also utilized in the preparation of agrochemicals and dyes, where its structural features contribute to improved stability and biological activity. Its amine functionality allows for easy derivatization, making it valuable in combinatorial chemistry and high-throughput screening for drug discovery.

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