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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)-

5,8,11,14-Eicosatetraenamide, N-(4-hydroxyphenyl)-,(5Z,8Z,11Z,14Z)-

CCCCC/C=CC/C=CC/C=CC/C=CCCCC(=O)Nc1ccc(cc1)O Request for Quotation
Chemical Name: 5,8,11,14-Eicosatetraenamide, N-(4-hydroxyphenyl)-,(5Z,8Z,11Z,14Z)-
CAS Number: 183718-77-6
Product Number: AG00AP3I(AGN-PC-0QCO88)
Synonyms:
MDL No:
Molecular Formula: C26H37NO2
Molecular Weight: 395.5775

Identification/Properties

Properties
Form:
Liquid
Computed Properties
Molecular Weight:
395.587g/mol
XLogP3:
7.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
15
Exact Mass:
395.282g/mol
Monoisotopic Mass:
395.282g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
29
Formal Charge:
0
Complexity:
511
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
4
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


The compound (5Z,8Z,11Z,14Z)-N-(4-Hydroxyphenyl)-5,8,11,14-eicosatetraenamide, also known by the systematic name N-(4-hydroxyphenyl) arachidonoylethanolamide, is a fatty acid amide derived from arachidonic acid and phenol. This specific compound has shown significant potential in chemical synthesis processes as a versatile building block due to its unique structure and reactivity.In chemical synthesis, (5Z,8Z,11Z,14Z)-N-(4-Hydroxyphenyl)-5,8,11,14-eicosatetraenamide can serve as a valuable precursor for the creation of novel molecules with diverse functionalities. Its long hydrocarbon chain and aromatic phenyl group provide opportunities for structural modifications through various chemical reactions such as acylation, alkylation, and cross-coupling reactions. Additionally, the presence of the hydroxyphenyl group enhances the compound's compatibility with different reaction conditions and allows for the introduction of additional functional groups.Furthermore, the conjugated polyunsaturated nature of the eicosatetraenamide moiety can contribute to the synthesis of compounds with specialized biological activities or therapeutic properties. By utilizing the unique features of this compound, chemists can design and synthesize a wide range of complex molecules for applications in medicinal chemistry, materials science, and organic synthesis.Overall, (5Z,8Z,11Z,14Z)-N-(4-Hydroxyphenyl)-5,8,11,14-eicosatetraenamide represents a valuable building block in chemical synthesis, offering opportunities for the creation of structurally diverse compounds with tailored properties and potential applications in various fields of chemistry.