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Home  > 2-(3-(Trifluoromethyl)phenyl)acetohydrazide

AI85949

116622-96-9 | 2-(3-(Trifluoromethyl)phenyl)acetohydrazide

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $212.00 $148.00 -   +
1g 95% in stock $388.00 $271.00 -   +
5g 95% in stock $1,092.00 $764.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AI85949
Chemical Name: 2-(3-(Trifluoromethyl)phenyl)acetohydrazide
CAS Number: 116622-96-9
Molecular Formula: C9H9F3N2O
Molecular Weight: 218.1758
MDL Number: MFCD11643284
SMILES: NNC(=O)Cc1cccc(c1)C(F)(F)F

 

Upstream Synthesis Route
  • 3-(Trifluoromethyl)benzeneacetic acid hydrazide, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it a valuable reagent for various synthetic reactions. One of the key applications of $name$ in chemical synthesis is as a building block for the preparation of heterocyclic compounds. By reacting with different reagents or undergoing cyclization reactions, $name$ can be utilized to synthesize a range of heterocycles, such as pyrazoles, triazoles, and oxazoles. These heterocyclic compounds have diverse pharmaceutical and agrochemical applications, making the use of $name$ crucial in drug discovery and development.Additionally, $name$ can be employed as a precursor for the synthesis of fluorine-containing compounds. The trifluoromethyl group in $name$ imparts unique properties to the resulting molecules, such as increased lipophilicity and metabolic stability. This makes $name$ a valuable starting material for the preparation of fluorinated pharmaceuticals, agrochemicals, and materials with enhanced bioactivity and chemical properties.Furthermore, $name$ has also been used in the development of ligands for transition metal catalyzed reactions. By incorporating $name$ into the structure of ligands, researchers can modulate the electronic and steric properties of the ligands, leading to improved catalytic activities and selectivities in various transformations, such as cross-coupling reactions, hydrogenation, and C-H activation.Overall, the application of 3-(Trifluoromethyl)benzeneacetic acid hydrazide in chemical synthesis offers a wide range of opportunities for the construction of complex molecules with potential pharmaceutical, agrochemical, and materials science applications.
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