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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-(diethoxymethyl)-

CCOC(c1cccc(c1)C=O)OCC Request for Quotation
Chemical Name: Benzaldehyde, 3-(diethoxymethyl)-
CAS Number: 150990-60-6
Product Number: AG001MYZ(AGN-PC-00UQKU)
Synonyms:
MDL No:
Molecular Formula: C12H16O3
Molecular Weight: 208.2536

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Chemical Structure


3-(Diethoxymethyl)benzaldehyde is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. In organic chemistry, it serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. The presence of both the aldehyde and diethoxymethyl functional groups makes it a crucial intermediate in the formation of intricate organic molecules. It can undergo different types of chemical transformations, such as acetal formation, which is essential for protecting aldehyde groups in multi-step synthesis. Additionally, its aromatic benzene ring provides opportunities for further derivatization, leading to the creation of diverse compounds with desired properties. The application of 3-(Diethoxymethyl)benzaldehyde in chemical synthesis enables chemists to design efficient routes for the synthesis of complex molecules and facilitates the development of new materials with potential applications across various industries.