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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-Methoxy-4,6-bis(trifluoromethyl)benzaldehyde

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Chemical Name: 2-Methoxy-4,6-bis(trifluoromethyl)benzaldehyde
CAS Number: 180134-14-9
Product Number: AG00I00C(AGN-PC-0WAOG4)
Synonyms:
MDL No: MFCD06660316
Molecular Formula:
Molecular Weight:

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Chemical Structure


2-Methoxy-4,6-bis(trifluoromethyl)benzaldehyde, a powerful aromatic aldehyde, finds significant application in the realm of chemical synthesis. This compound serves as a versatile building block and intermediate in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties. Its trifluoromethyl groups confer enhanced stability and reactivity, enabling it to participate in a wide range of reactions such as nucleophilic addition, condensation, and metal-catalyzed transformations. Furthermore, the methoxy group provides additional functionalization opportunities, allowing for the modulation of its physicochemical properties. Overall, 2-Methoxy-4,6-bis(trifluoromethyl)benzaldehyde stands as a valuable tool in the hands of synthetic chemists seeking to craft intricate molecular structures and innovate in the realm of organic chemistry.