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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)-

2,5-Furandione, 3-(acetyloxy)dihydro-

CC(=O)OC1CC(=O)OC1=O Request for Quotation
Chemical Name: 2,5-Furandione, 3-(acetyloxy)dihydro-
CAS Number: 24766-96-9
Product Number: AG002PEB(AGN-PC-0CM5MN)
Synonyms:
MDL No:
Molecular Formula: C6H6O5
Molecular Weight: 158.1088

Identification/Properties

Properties
MP:
83-85°C
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
158.109g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
158.022g/mol
Monoisotopic Mass:
158.022g/mol
Topological Polar Surface Area:
69.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
219
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


The compound 2,5-Furandione, 3-(acetyloxy)dihydro- is utilized in chemical synthesis as a versatile building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique molecular structure allows for the creation of complex organic compounds with specific functional groups and properties. This compound serves as a key intermediate in the synthesis of a wide range of valuable products, playing a crucial role in the development and diversification of chemical processes. By incorporating 2,5-Furandione, 3-(acetyloxy)dihydro- into synthetic routes, chemists can access new pathways for the efficient production of novel compounds with potential applications in multiple industries.