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58914-35-5

2-Formyl-3-(trifluoromethyl)phenol, 2-Formyl-3-hydroxybenzotrifluoride, 6-(Trifluoromethyl)salicylaldehyde

Catalog#: AR00EGQH  |   CAS#: 58914-35-5  |   MDL#: MFCD16999701  |   MF: C8H5F3O2  |   MW: 190.11930959999995

Packsize Purity Price Availability Quantity
100mg 98% $13.00 Global Stock Buy Now Add To Cart
250mg 98% $19.00 Global Stock Buy Now Add To Cart
1g 98% $61.00 Global Stock Buy Now Add To Cart
5g 98% $283.00 Global Stock Buy Now Add To Cart
10g 98% $523.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00EGQH
Chemical Name 2-Formyl-3-(trifluoromethyl)phenol, 2-Formyl-3-hydroxybenzotrifluoride, 6-(Trifluoromethyl)salicylaldehyde
CAS Number 58914-35-5
Molecular Formula C8H5F3O2
Molecular Weight 190.11930959999995
MDL Number MFCD16999701
SMILES O=Cc1c(O)cccc1C(F)(F)F

2-Hydroxy-6-(trifluoromethyl)benzaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in organic chemistry due to its unique structure and reactivity.In chemical synthesis, 2-Hydroxy-6-(trifluoromethyl)benzaldehyde serves as a key starting material for the preparation of various important compounds. Its aldehyde group allows for selective functionalization reactions, enabling the creation of new carbon-carbon and carbon-heteroatom bonds. The presence of the hydroxyl and trifluoromethyl groups further enhances the reactivity of this compound, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.Moreover, 2-Hydroxy-6-(trifluoromethyl)benzaldehyde can undergo various transformations such as condensation, reduction, and oxidation reactions to generate a wide array of derivatives with diverse chemical properties. These derivatives can exhibit unique biological activities or serve as intermediates in the preparation of complex organic molecules.Overall, the application of 2-Hydroxy-6-(trifluoromethyl)benzaldehyde in chemical synthesis allows for the efficient and selective construction of intricate molecular structures, making it an indispensable tool for synthetic chemists in the pursuit of novel compounds with valuable properties and functions.
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