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58536-48-4

(2-METHYL-2H-INDAZOL-3-YL)METHANOL

Catalog#: AR00EEW9  |   CAS#: 58536-48-4  |   MDL#: MFCD08060471  |   MF: C9H10N2O  |   MW: 162.1885

Packsize Purity Price Availability Quantity
100mg 98% $10.00 Global Stock Buy Now Add To Cart
250mg 98% $11.00 Global Stock Buy Now Add To Cart
1g 98% $40.00 Global Stock Buy Now Add To Cart
5g 98% $182.00 Global Stock Buy Now Add To Cart
10g 98% $301.00 Global Stock Buy Now Add To Cart
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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.
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GHS Pictogram N/A
UN# -
Hazard Statements -
Class -
Packing Group -

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