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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-Butenedioic acid (2Z)-, di-2-propenyl ester

C=CC/C(=C(/C(=O)O)CC=C)/C(=O)O.C=CCOC(=O)/C=CC(=O)OCC=C Request for Quotation
Chemical Name: 2-Butenedioic acid (2Z)-, di-2-propenyl ester
CAS Number: 999-21-3
Product Number: AG003VLP(AGN-PC-0WA04Q)
Synonyms:
MDL No:
Molecular Formula: C20H24O8
Molecular Weight: 392.3998

Identification/Properties

Properties
MP:
-47°C
BP:
263.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
196.202g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
196.074g/mol
Monoisotopic Mass:
196.074g/mol
Topological Polar Surface Area:
52.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
227
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
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


Diallyl Maleate is a versatile chemical compound commonly used in chemical synthesis for its unique reactivity and properties. In particular, it is widely utilized in the synthesis of various polymers, resins, and coatings due to its ability to form cross-linked structures. Additionally, Diallyl Maleate serves as a valuable comonomer in copolymerization reactions, enhancing the mechanical strength, thermal stability, and chemical resistance of the resulting materials. Its reactive double bonds allow for further functionalization and modification, making it a valuable building block in the production of specialty chemicals and advanced materials. In the realm of chemical synthesis, Diallyl Maleate plays a crucial role in the development of innovative products with tailored properties for a wide range of industrial applications.