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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)-

Ethanone, 1-(3,5-dimethyl-2-furanyl)-

Cc1cc(c(o1)C(=O)C)C Request for Quotation
Chemical Name: Ethanone, 1-(3,5-dimethyl-2-furanyl)-
CAS Number: 22940-86-9
Product Number: AG002LM9(AGN-PC-0JT802)
Synonyms:
MDL No:
Molecular Formula: C8H10O2
Molecular Weight: 138.1638

Identification/Properties

Properties
MP:
18℃
BP:
209.8°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
138.166g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
138.068g/mol
Monoisotopic Mass:
138.068g/mol
Topological Polar Surface Area:
30.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
142
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


1-(3,5-Dimethylfuran-2-yl)ethanone is a versatile compound commonly used in chemical synthesis due to its unique properties. This compound is known for its ability to act as a precursor in the preparation of various organic molecules. It serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.In organic synthesis, 1-(3,5-Dimethylfuran-2-yl)ethanone can undergo a variety of reactions such as acylation, alkylation, and condensation reactions to produce a wide range of derivatives. These derivatives can exhibit different chemical and physical properties, making them valuable intermediates in the production of complex organic compounds.The presence of the furan ring in 1-(3,5-Dimethylfuran-2-yl)ethanone also imparts unique reactivity, allowing it to participate in various cyclization reactions to form heterocyclic compounds. These heterocycles have diverse applications in medicinal chemistry, materials science, and other fields.Overall, the versatility and reactivity of 1-(3,5-Dimethylfuran-2-yl)ethanone make it a valuable tool in chemical synthesis, enabling the efficient and cost-effective preparation of a wide range of organic molecules with diverse applications.