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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)-

4-Pentenoic acid, 2,2-dimethyl-, ethyl ester

CCOC(=O)C(CC=C)(C)C Request for Quotation
Chemical Name: 4-Pentenoic acid, 2,2-dimethyl-, ethyl ester
CAS Number: 86549-27-1
Product Number: AG00H3LA(AGN-PC-00KXWT)
Synonyms:
MDL No:
Molecular Formula: C9H16O2
Molecular Weight: 156.22214

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Chemical Structure


In chemical synthesis, Ethyl 2,2-dimethylpent-4-enoate, also known as $name$, serves as a versatile building block for the creation of various organic compounds. This compound is particularly valued for its ability to participate in reactions such as esterification, Grignard reactions, and conjugate addition. With its unique structure and reactivity, Ethyl 2,2-dimethylpent-4-enoate can be utilized as a key intermediate in the synthesis of pharmaceuticals, fragrances, and agrochemicals. Its presence in the chemical toolbox enables the construction of complex molecular structures and the development of innovative chemical pathways.