
Catalog Number	AR00EEW9
Chemical Name	(2-Methyl-2H-indazol-3-yl)methanol
CAS Number	58536-48-4
Molecular Formula	C9H10N2O
Molecular Weight	162.1885
MDL Number	MFCD08060471
SMILES	OCc1n(C)nc2c1cccc2

The compound (2-Methyl-2H-indazol-3-yl)methanol, also known as $name$, is a versatile building block in chemical synthesis. Its unique structure and reactivity make it a valuable tool for organic chemists seeking to create complex molecules. When utilized in synthesis, $name$ serves as a key intermediate in the formation of various pharmaceuticals, agrochemicals, and specialty chemicals.One of the primary applications of (2-Methyl-2H-indazol-3-yl)methanol in chemical synthesis is its use as a nucleophilic reagent in carbon-carbon bond formation reactions. By acting as a nucleophile, $name$ can participate in various carbon-carbon bond-forming reactions such as Grignard, Suzuki-Miyaura, or Heck coupling reactions. These transformations allow chemists to construct intricate carbon frameworks with high efficiency and precision.Furthermore, (2-Methyl-2H-indazol-3-yl)methanol can also serve as a versatile starting material for the synthesis of heterocyclic compounds. The indazole moiety in $name$ provides a unique scaffold that imparts specific chemical and biological properties to the final products. Chemists can leverage this characteristic to access diverse classes of heterocycles with potential applications in medicinal chemistry and materials science.Overall, the application of (2-Methyl-2H-indazol-3-yl)methanol in chemical synthesis offers a wide range of possibilities for the creation of novel molecules with tailored properties. Its strategic use as a key intermediate in organic transformations underscores its significance in advancing the field of synthetic chemistry.