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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)-

Ethanone, 1-(5-hydroxy-2-methoxyphenyl)-

COc1ccc(cc1C(=O)C)O Request for Quotation
Chemical Name: Ethanone, 1-(5-hydroxy-2-methoxyphenyl)-
CAS Number: 31405-60-4
Product Number: AG00CYOU(AGN-PC-000LUH)
Synonyms:
MDL No:
Molecular Formula: C9H10O3
Molecular Weight: 166.1739

Identification/Properties

Computed Properties
Molecular Weight:
166.176g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
166.063g/mol
Monoisotopic Mass:
166.063g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
167
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


The 1-(5-Hydroxy-2-methoxyphenyl)ethanone is a versatile organic compound commonly used in chemical synthesis. It serves as a crucial building block in the production of various pharmaceuticals, fragrances, and natural products due to its unique structural properties. This compound acts as a key intermediate in the synthesis of complex organic molecules, facilitating the creation of novel compounds with valuable biological activities. By incorporating 1-(5-Hydroxy-2-methoxyphenyl)ethanone into chemical reactions, chemists can efficiently construct intricate molecular structures, leading to the development of new drugs, flavors, and fragrance compounds. Its strategic placement in synthetic pathways enables the controlled modification of functional groups, resulting in the targeted synthesis of diverse compounds with enhanced properties. Additionally, the incorporation of 1-(5-Hydroxy-2-methoxyphenyl)ethanone in multi-step syntheses allows for the rapid and efficient assembly of structurally complex molecules, making it a valuable tool for chemical researchers and professionals seeking to innovate in various industries.