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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)-

Phenol, 4-tetradecyl-

CCCCCCCCCCCCCCc1ccc(cc1)O Request for Quotation
Chemical Name: Phenol, 4-tetradecyl-
CAS Number: 25401-89-2
Product Number: AG003855(AGN-PC-0JLKU9)
Synonyms:
MDL No:
Molecular Formula: C20H34O
Molecular Weight: 290.4834

Identification/Properties

Computed Properties
Molecular Weight:
290.491g/mol
XLogP3:
8.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
13
Exact Mass:
290.261g/mol
Monoisotopic Mass:
290.261g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
206
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
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


4-Tetradecylphenol, known for its chemical versatility, is commonly utilized in a wide range of chemical synthesis applications. This compound is particularly valued for its ability to act as a surfactant in various reactions, aiding in the dispersion and solubilization of different compounds across a range of solvents. Additionally, 4-Tetradecylphenol serves as a valuable building block in the creation of specialized polymers, resins, and coatings due to its unique structure and reactivity. In organic synthesis, it can function as a precursor for the modification of other molecules, allowing for the introduction of specific functional groups or structural changes. Furthermore, its amphiphilic nature makes it a useful component in the formulation of emulsions and dispersants, finding application in industries such as pharmaceuticals, agrochemicals, and cosmetics.