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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-[(2-naphthalenyloxy)methyl]-

OC(=O)c1ccc(o1)COc1ccc2c(c1)cccc2 Request for Quotation
Chemical Name: 2-Furancarboxylic acid, 5-[(2-naphthalenyloxy)methyl]-
CAS Number: 296274-02-7
Product Number: AG00JKEY(AGN-PC-0JVIFZ)
Synonyms:
MDL No:
Molecular Formula: C16H12O4
Molecular Weight: 268.2641

Identification/Properties

Computed Properties
Molecular Weight:
268.268g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
268.074g/mol
Monoisotopic Mass:
268.074g/mol
Topological Polar Surface Area:
59.7A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
343
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


5-[(2-Naphthalenyloxy)methyl]-2-furancarboxylic acid is a versatile compound widely used in chemical synthesis as a key building block for various organic reactions. Its unique structure, containing both a furan ring and a naphthalene group, enables it to participate in diverse chemical transformations.One important application of this compound is as a precursor for the synthesis of novel drug candidates. By utilizing the functional groups present in 5-[(2-Naphthalenyloxy)methyl]-2-furancarboxylic acid, chemists can introduce different substituents or modify the core structure to develop potential pharmaceutical agents with enhanced biological activities.Additionally, this compound can be employed in the preparation of advanced materials such as polymers and organic electronics. Its ability to undergo selective functionalization and form complex molecular architectures makes it a valuable tool for designing materials with tailored properties and functionalities.Moreover, 5-[(2-Naphthalenyloxy)methyl]-2-furancarboxylic acid serves as a starting material for the synthesis of organic dyes and pigments. By manipulating its molecular structure, chemists can access a range of chromophores with varied colors and optical properties, suitable for applications in textile dyes, inks, and colorants.In summary, the versatility of 5-[(2-Naphthalenyloxy)methyl]-2-furancarboxylic acid in chemical synthesis makes it an indispensable component in the toolbox of synthetic chemists, enabling the efficient construction of complex molecules with diverse applications in pharmaceuticals, materials science, and dye chemistry.