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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)-

Hexanoic acid, 2-ethyl-, decyl ester

CCCCCCCCCCOC(=O)C(CCCC)CC Request for Quotation
Chemical Name: Hexanoic acid, 2-ethyl-, decyl ester
CAS Number: 93777-46-9
Product Number: AG006E9C(AGN-PC-0JSNWV)
Synonyms:
MDL No:
Molecular Formula: C18H36O2
Molecular Weight: 284.4772

Identification/Properties

Properties
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Decyl 2-ethylhexanoate is a versatile compound that finds extensive application in chemical synthesis processes. As a key ingredient, it serves as an efficient ester in various reactions, contributing to the formation of a wide range of organic compounds. This compound is valued for its ability to act as a solvent, a reaction medium, or a precursor in synthetic pathways across different industries. By participating in esterification, transesterification, and other chemical reactions, Decyl 2-ethylhexanoate plays a crucial role in creating new molecules with distinct properties and functionalities. Its compatibility with a variety of starting materials and reaction conditions makes it a valuable tool for chemists and researchers seeking to design and develop novel compounds with tailored characteristics.