(1-Trityl-1H-Pyrazol-4-Yl)Methanol

95%

Reagent Code: #84768
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CAS Number 88529-69-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 340.42 g/mol
Formula C₂₃H₂₀N₂O
badge Registry Numbers
MDL Number MFCD29917021
thermostat Physical Properties
Boiling Point 544.7±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.10±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

(1-Trityl-1H-Pyrazol-4-Yl)Methanol is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring a trityl-protected pyrazole moiety, makes it valuable in the development of pharmaceuticals and bioactive compounds. It is often employed in the synthesis of complex molecules, particularly in medicinal chemistry, where it serves as a building block for designing drug candidates. The trityl group provides stability during reactions, allowing selective modifications to the pyrazole ring. This compound is also explored in the creation of ligands for metal-catalyzed reactions, contributing to advancements in catalysis and material science. Its applications extend to the study of enzyme inhibitors and receptor modulators, aiding in the discovery of new therapeutic agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days $363.26
inventory 250mg
10-20 days $716.49
inventory 1g
10-20 days $1,432.98
(1-Trityl-1H-Pyrazol-4-Yl)Methanol
(1-Trityl-1H-Pyrazol-4-Yl)Methanol is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring a trityl-protected pyrazole moiety, makes it valuable in the development of pharmaceuticals and bioactive compounds. It is often employed in the synthesis of complex molecules, particularly in medicinal chemistry, where it serves as a building block for designing drug candidates. The trityl group provides stability during reactions, allowing selective modifications to the pyrazole ring. This compound is also explored in the creation of ligands for metal-catalyzed reactions, contributing to advancements in catalysis and material science. Its applications extend to the study of enzyme inhibitors and receptor modulators, aiding in the discovery of new therapeutic agents.
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