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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)-

2-Furancarboxylic acid, 5-(tetradecyloxy)-

CCCCCCCCCCCCCCOc1ccc(o1)C(=O)O Request for Quotation
Chemical Name: 2-Furancarboxylic acid, 5-(tetradecyloxy)-
CAS Number: 54857-86-2
Product Number: AG00D7YZ(AGN-PC-0JLJWL)
Synonyms:
MDL No: MFCD01726059
Molecular Formula: C19H32O4
Molecular Weight: 324.4550

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
324.461g/mol
XLogP3:
7.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
15
Exact Mass:
324.23g/mol
Monoisotopic Mass:
324.23g/mol
Topological Polar Surface Area:
59.7A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
293
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 5-(Tetradecyloxy)-2-furoic acid, also known as $name$, serves as a valuable reagent in chemical synthesis processes. With its unique structure and properties, this compound finds significant utility in organic chemistry applications. Specifically, $name$ is used as a versatile building block for the synthesis of various organic compounds, owing to its ability to undergo different chemical reactions and transformations.One of the key applications of 5-(Tetradecyloxy)-2-furoic acid in chemical synthesis is its role as a precursor in the preparation of novel heterocyclic compounds. Through various synthetic pathways, $name$ can be manipulated to introduce functional groups and structural motifs that are crucial for the design and development of new molecules with desired properties. This compound acts as a strategic starting material for the construction of complex organic frameworks, enabling chemists to access a diverse range of molecular structures efficiently.Moreover, 5-(Tetradecyloxy)-2-furoic acid is employed in the synthesis of bioactive compounds and pharmaceutical intermediates. By utilizing the reactivity of $name$ in conjunction with other reagents and reaction conditions, chemists can carry out selective transformations to modify the furoic acid core and tailor the molecular properties for specific applications. This synthesis strategy enables the creation of targeted compounds with potential biological activity, paving the way for the development of new drug candidates and chemical probes.Overall, the versatile nature of 5-(Tetradecyloxy)-2-furoic acid makes it a valuable tool in chemical synthesis, offering opportunities for creative molecule design and efficient preparation of diverse organic compounds. Whether used in the construction of heterocyclic frameworks or the synthesis of bioactive molecules, this compound plays a crucial role in advancing the field of organic chemistry and pharmaceutical research.