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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, 4-(hydroxymethyl)-

OCc1ccc(cc1)CC(=O)O Request for Quotation
Chemical Name: Benzeneacetic acid, 4-(hydroxymethyl)-
CAS Number: 73401-74-8
Product Number: AG005O7F(AGN-PC-0KRQXD)
Synonyms:
MDL No:
Molecular Formula: C9H10O3
Molecular Weight: 166.1739

Identification/Properties

Properties
MP:
131-134 °C(lit.)
BP:
357.841 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
166.176g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
166.063g/mol
Monoisotopic Mass:
166.063g/mol
Topological Polar Surface Area:
57.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
148
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-(4-(Hydroxymethyl)phenyl)acetic acid, also known as $name$, is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a key building block in organic chemistry, particularly in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. In chemical synthesis, $name$ can be utilized as a valuable intermediate to introduce the hydroxymethyl functional group into organic molecules. This hydroxymethyl group is crucial for enhancing the solubility, stability, and biological activity of the final products. Furthermore, the phenyl ring in $name$ provides aromaticity and structural diversity, making it a versatile scaffold for the design of new compounds.One of the key applications of 2-(4-(Hydroxymethyl)phenyl)acetic acid is in the development of novel drug candidates. By incorporating this compound into the chemical structure of potential drugs, researchers can modulate the pharmacokinetic properties, improve target specificity, and enhance the overall efficacy of the pharmaceuticals. Additionally, the presence of the hydroxymethyl group offers opportunities for further functionalization through various chemical reactions, enabling the synthesis of a wide range of derivatives with tailored properties.Overall, the strategic incorporation of 2-(4-(Hydroxymethyl)phenyl)acetic acid in chemical synthesis opens up new avenues for designing innovative compounds with diverse applications in the fields of medicine, agriculture, and materials science.