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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)-

Benzenemethanol, 2-fluoro-4-hydroxy-

OCc1ccc(cc1F)O Request for Quotation
Chemical Name: Benzenemethanol, 2-fluoro-4-hydroxy-
CAS Number: 96740-92-0
Product Number: AG00IJUU(AGN-PC-0A0SBR)
Synonyms:
MDL No:
Molecular Formula: C7H7FO2
Molecular Weight: 142.1277

Identification/Properties

Computed Properties
Molecular Weight:
142.129g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
142.043g/mol
Monoisotopic Mass:
142.043g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
108
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


3-Fluoro-4-(hydroxymethyl)phenol, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in various reactions due to its unique properties and functional groups. Its primary application lies in organic chemistry, where it serves as a key building block for the synthesis of complex molecules and pharmaceuticals. One important use of 3-Fluoro-4-(hydroxymethyl)phenol is as a starting material for the synthesis of biologically active compounds. Its fluoro and hydroxymethyl groups can be selectively modified through various chemical reactions to introduce specific functionalities into the target molecules. This versatility makes it a valuable tool for designing and manufacturing new drugs and agrochemicals.Additionally, 3-Fluoro-4-(hydroxymethyl)phenol can serve as a protecting group in organic synthesis. By temporarily shielding sensitive functional groups in a molecule, this compound enables chemists to carry out selective reactions without unwanted side reactions. Once the desired transformations are complete, the protecting group can be easily removed, revealing the reactive groups for further modifications. Furthermore, the presence of a fluoro substituent in 3-Fluoro-4-(hydroxymethyl)phenol imparts unique properties to the synthesized compounds, such as altered reactivity, lipophilicity, and biological activity. These attributes are advantageous in medicinal chemistry for enhancing drug efficacy, improving pharmacokinetics, and reducing side effects.In summary, 3-Fluoro-4-(hydroxymethyl)phenol is a versatile and indispensable compound in chemical synthesis, offering a wide range of applications in organic chemistry, drug discovery, and materials science. Its strategic use as a building block, protecting group, and bioisostere underscores its significance in modern chemical research and development.