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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)-

Benzaldehyde, 3-(difluoromethoxy)-4-methoxy-

COc1ccc(cc1OC(F)F)C=O Request for Quotation
Chemical Name: Benzaldehyde, 3-(difluoromethoxy)-4-methoxy-
CAS Number: 153587-11-2
Product Number: AG007HQ5(AGN-PC-0L19OO)
Synonyms:
MDL No:
Molecular Formula: C9H8F2O3
Molecular Weight: 202.1548

Identification/Properties

Computed Properties
Molecular Weight:
202.157g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
202.044g/mol
Monoisotopic Mass:
202.044g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
187
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


3-(Difluoromethoxy)-4-methoxybenzaldehyde, also known in the chemical world as $name$, serves as a versatile building block in chemical synthesis. This compound plays a crucial role as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure, featuring difluoromethoxy and methoxy functional groups, imparts valuable properties that enhance the reactivity and selectivity of synthetic processes. In particular, 3-(Difluoromethoxy)-4-methoxybenzaldehyde is utilized in the creation of complex organic molecules through C-C and C-N bond formation, making it an indispensable component in the toolkit of organic chemists. With its ability to facilitate the construction of diverse molecular architectures, this compound underscores its significance as a foundational element in modern chemical synthesis methodologies.