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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)-

Phosphonic acid, 3-butenyl-, diethyl ester

CCOP(=O)(OCC)CCC=C Request for Quotation
Chemical Name: Phosphonic acid, 3-butenyl-, diethyl ester
CAS Number: 15916-48-0
Product Number: AG001QJM(AGN-PC-0NE680)
Synonyms:
MDL No:
Molecular Formula: C8H17O3P
Molecular Weight: 192.1925

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Chemical Structure


Diethyl 3-butenylphosphonate is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. With its double bond and phosphonate group, this compound serves as a valuable building block in the preparation of various organic molecules through diverse synthetic pathways. In particular, Diethyl 3-butenylphosphonate is frequently employed in the development of pharmaceuticals, agrochemicals, and materials due to its ability to undergo a range of chemical transformations, such as nucleophilic additions, radical reactions, and transition metal-catalyzed processes. Its structural features make it an essential component in the creation of complex molecular structures with high efficiency and selectivity, making it a key tool for chemists in the design and synthesis of novel compounds with desired properties.