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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, dihydro-3-(nonenyl)-

CCCCCCCC=CC1CC(=O)OC1=O Request for Quotation
Chemical Name: 2,5-Furandione, dihydro-3-(nonenyl)-
CAS Number: 28928-97-4
Product Number: AG002X3I(AGN-PC-0JO70T)
Synonyms:
MDL No:
Molecular Formula: C13H20O3
Molecular Weight: 224.2961

Identification/Properties

Properties
BP:
126-130 °C0.15 mm Hg(lit.)
Stability:
Moisture Sensitive
Refractive Index:
n20/D 1.476
Computed Properties
Molecular Weight:
224.3g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
7
Exact Mass:
224.141g/mol
Monoisotopic Mass:
224.141g/mol
Topological Polar Surface Area:
43.4A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
268
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
1
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


Nonenylsuccinic anhydride is commonly used in chemical synthesis as a versatile building block for the modification of various organic compounds. Its reactive anhydride functionality allows for the introduction of nonenyl groups into organic molecules, enabling the creation of new compounds with tailored properties. This compound is particularly utilized in the synthesis of surfactants, polymers, and advanced materials due to its ability to undergo facile reactions with nucleophiles. By incorporating nonenylsuccinic anhydride into chemical reactions, researchers and chemists can effectively functionalize organic molecules to enhance their reactivity, solubility, and overall performance in a wide range of applications.