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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-(2-fluoro-4-hydroxyphenyl)-

Oc1ccc(c(c1)F)C(=O)C Request for Quotation
Chemical Name: Ethanone, 1-(2-fluoro-4-hydroxyphenyl)-
CAS Number: 98619-07-9
Product Number: AG00329R(AGN-PC-0KK0HK)
Synonyms:
MDL No:
Molecular Formula: C8H7FO2
Molecular Weight: 154.1384

Identification/Properties

Properties
MP:
120-124 °C
BP:
292.7±20.0°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
154.14g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
154.043g/mol
Monoisotopic Mass:
154.043g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
158
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


1-(2-fluoro-4-hydroxyphenyl)ethanone is a versatile compound commonly used in chemical synthesis as a key intermediate for the preparation of various organic compounds. It serves as a crucial building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.This compound is particularly valuable in the creation of biologically active molecules due to its unique structural properties. Its functional groups offer a wide range of reactivity, allowing for the introduction of different substituents and modifications to tailor the properties of the final product.In chemical synthesis, 1-(2-fluoro-4-hydroxyphenyl)ethanone can undergo various reactions such as acylation, alkylation, and condensation reactions to form more complex structures. These transformations enable chemists to design and produce compounds with specific desired characteristics, making it an indispensable tool in the field of organic chemistry.Overall, the utility of 1-(2-fluoro-4-hydroxyphenyl)ethanone in chemical synthesis lies in its ability to act as a crucial intermediate for the efficient and strategic construction of diverse organic molecules with potential applications in various industries.