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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-hydroxy-4-methoxy-, methyl ester

COC(=O)Cc1ccc(c(c1)O)OC Request for Quotation
Chemical Name: Benzeneacetic acid, 3-hydroxy-4-methoxy-, methyl ester
CAS Number: 15964-81-5
Product Number: AG001R9K(AGN-PC-0N4WAV)
Synonyms:
MDL No:
Molecular Formula: C10H12O4
Molecular Weight: 196.1999

Identification/Properties

Computed Properties
Molecular Weight:
196.202g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
196.074g/mol
Monoisotopic Mass:
196.074g/mol
Topological Polar Surface Area:
55.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
193
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


Methyl 3-Hydroxy-4-methoxyphenylacetate, also known as $name$, serves as a versatile building block in chemical synthesis processes. This compound is a key intermediate that is widely utilized in the pharmaceutical and agrochemical industries for the production of various important organic compounds.Its unique chemical properties make it a valuable precursor in the synthesis of complex molecules, such as pharmaceutical drugs, agrochemicals, and specialty chemicals. $name$ is often employed as a starting material for the preparation of biologically active compounds with diverse applications.In chemical synthesis, $name$ can undergo various transformations, including esterification, oxidation, reduction, and functional group interconversions, to yield structurally diverse molecules with desired properties. Its versatility and reactivity make it a crucial component in the creation of novel compounds with potential therapeutic, agricultural, or industrial benefits.Chemists and researchers leverage the utility of Methyl 3-Hydroxy-4-methoxyphenylacetate to construct intricate molecular structures, optimize chemical reactions, and develop innovative synthetic routes for the efficient and sustainable production of valuable compounds. Its role in chemical synthesis highlights its significance as a valuable tool for advancing scientific research and technological innovation in diverse fields.