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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)-

Benzeneacetic acid, 3-phenoxy-

OC(=O)Cc1cccc(c1)Oc1ccccc1 Request for Quotation
Chemical Name: Benzeneacetic acid, 3-phenoxy-
CAS Number: 32852-81-6
Product Number: AG0033S1(AGN-PC-0JMS78)
Synonyms:
MDL No:
Molecular Formula: C14H12O3
Molecular Weight: 228.2433

Identification/Properties

Properties
MP:
88-91 °C(lit.)
BP:
385.378 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
228.247g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
228.079g/mol
Monoisotopic Mass:
228.079g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
246
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


2-(3-Phenoxyphenyl)acetic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a crucial building block in the production of various pharmaceuticals, agrochemicals, and materials. Its unique chemical structure and reactivity make it a valuable intermediate in the synthesis of complex organic molecules.One of the key applications of 2-(3-Phenoxyphenyl)acetic acid is in the pharmaceutical industry, where it is utilized in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive compounds. Its presence in the molecular structure of these drugs imparts specific pharmacological properties, making it an essential component of their synthesis.Additionally, 2-(3-Phenoxyphenyl)acetic acid finds extensive use in the preparation of specialty chemicals and materials. Its ability to undergo various chemical transformations, such as esterification, amidation, and oxidation, allows for the production of a diverse range of derivatives with tailored properties for specific applications.In chemical synthesis, this compound serves as a versatile starting material for the construction of more complex molecules through strategic functional group manipulations. Its presence in the synthesis pathway enables chemists to introduce specific functionalities and stereochemical elements, contributing to the overall efficiency and selectivity of the synthetic process.Overall, the versatile nature of 2-(3-Phenoxyphenyl)acetic acid makes it a valuable tool in chemical synthesis, enabling the creation of novel compounds with unique properties and applications in various industrial sectors.