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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)-

Benzoic acid, 3-(4-hydroxyphenoxy)-

Oc1ccc(cc1)Oc1cccc(c1)C(=O)O Request for Quotation
Chemical Name: Benzoic acid, 3-(4-hydroxyphenoxy)-
CAS Number: 35065-12-4
Product Number: AG0038SV(AGN-PC-0JPNBD)
Synonyms:
MDL No:
Molecular Formula: C13H10O4
Molecular Weight: 230.2161

Identification/Properties

Computed Properties
Molecular Weight:
230.219g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
230.058g/mol
Monoisotopic Mass:
230.058g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
258
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 3-(4'-Hydroxy)phenoxybenzoic Acid is a versatile compound widely used in chemical synthesis. Its primary application lies in its utility as a building block for the synthesis of various organic compounds. Due to its unique structure and reactivity, this acid serves as a key intermediate in the production of a range of pharmaceuticals, agrochemicals, and materials.One of the main uses of 3-(4'-Hydroxy)phenoxybenzoic Acid is in the synthesis of specialized polymers and copolymers. By incorporating this compound into the polymerization process, researchers can tailor the properties of the resulting materials, such as thermal stability, chemical resistance, and mechanical strength. This acid's presence in the polymer backbone can enhance the overall performance characteristics of the final product.Furthermore, 3-(4'-Hydroxy)phenoxybenzoic Acid is essential for the creation of novel organic compounds with specific biological activities. By functionalizing the acid group or modifying the aromatic ring, chemists can design molecules with targeted properties for potential pharmaceutical applications. This acid's structural features make it a valuable starting material for designing drug candidates that exhibit desired therapeutic effects.Additionally, this acid plays a crucial role in the development of liquid crystals and dyes. Through strategic chemical modifications, researchers can utilize 3-(4'-Hydroxy)phenoxybenzoic Acid to synthesize molecules with unique optical properties, enabling the production of advanced display technologies and colorants. The acid's ability to influence the molecular arrangement and electronic interactions within these materials makes it indispensable in the field of molecular electronics and optoelectronics.