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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)-

Tetradecanoic acid, 2-ethylhexyl ester

CCCCCCCCCCCCCC(=O)OCC(CCCC)CC Request for Quotation
Chemical Name: Tetradecanoic acid, 2-ethylhexyl ester
CAS Number: 29806-75-5
Product Number: AG0033AS(AGN-PC-0JLNZI)
Synonyms:
MDL No:
Molecular Formula: C22H44O2
Molecular Weight: 340.5836

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
340.592g/mol
XLogP3:
9.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
19
Exact Mass:
340.334g/mol
Monoisotopic Mass:
340.334g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
263
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
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


2-Ethylhexyl myristate, also known as octyl myristate, is a versatile chemical compound commonly used in chemical synthesis as a reaction solvent and starting material. Due to its ability to dissolve a wide range of organic compounds, it is frequently employed as a solvent in various chemical reactions and processes. This compound is particularly valued for its properties, such as low toxicity, high stability, and compatibility with a variety of other chemicals. In chemical synthesis, 2-Ethylhexyl myristate serves as an effective medium for carrying out reactions that involve the modification or transformation of organic substrates. Its use in synthesis processes enables efficient mixing of reactants, facilitating the formation of desired products. Additionally, the ability of 2-Ethylhexyl myristate to act as a reaction medium can enhance the yield and selectivity of certain chemical reactions. Its versatility and compatibility make it a valuable ingredient in the toolkit of chemists and researchers engaged in diverse areas of chemical synthesis.