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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)-

5-methoxy-2-(trifluoromethyl)benzaldehyde

O=Cc1cc(OC)ccc1C(F)(F)F Request for Quotation
Chemical Name: 5-methoxy-2-(trifluoromethyl)benzaldehyde
CAS Number: 944905-42-4
Product Number: AG00IIA6(AGN-PC-0BSJCC)
Synonyms:
MDL No:
Molecular Formula: C9H7F3O2
Molecular Weight: 204.1459

Identification/Properties

Computed Properties
Molecular Weight:
204.148g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
204.04g/mol
Monoisotopic Mass:
204.04g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
203
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Methoxy-2-(trifluoromethyl)benzaldehyde is a versatile compound widely used in chemical synthesis as a key building block for the creation of various organic molecules. With its unique structure combining a methoxy group with a trifluoromethyl moiety attached to a benzaldehyde core, this compound offers numerous opportunities for designing and generating complex chemical structures.In chemical synthesis, 5-Methoxy-2-(trifluoromethyl)benzaldehyde serves as a valuable starting material for the synthesis of pharmaceuticals, agrochemicals, and materials with specific properties. Its ability to undergo diverse chemical transformations, including condensation reactions, nucleophilic additions, and substitutions, allows for the efficient modification and functionalization of its structure to introduce new chemical functionalities.Furthermore, the trifluoromethyl group in 5-Methoxy-2-(trifluoromethyl)benzaldehyde imparts unique physicochemical properties to the resulting compounds, such as enhanced lipophilicity, metabolic stability, and bioactivity, making it a valuable tool in drug discovery and development. Additionally, the methoxy group can serve as a directing group in organic reactions, facilitating regioselective transformations and improving overall synthetic efficiency.Overall, the diverse applications of 5-Methoxy-2-(trifluoromethyl)benzaldehyde in chemical synthesis underscore its significance as a valuable building block for the construction of complex molecules with tailored properties and functionalities.