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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)-

Phenol, 2-fluoro-4-methoxy-

COc1ccc(c(c1)F)O Request for Quotation
Chemical Name: Phenol, 2-fluoro-4-methoxy-
CAS Number: 167683-93-4
Product Number: AG001XIO(AGN-PC-0KKW8P)
Synonyms:
MDL No:
Molecular Formula: C7H7FO2
Molecular Weight: 142.1277

Identification/Properties

Properties
BP:
199.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Refractive Index:
1.5240-1.5280
Computed Properties
Molecular Weight:
142.129g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
142.043g/mol
Monoisotopic Mass:
142.043g/mol
Topological Polar Surface Area:
29.5A^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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Fluoro-4-methoxyphenol, or $name$, is a versatile compound widely utilized in chemical synthesis due to its unique properties. In organic chemistry, this compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its strategic placement of a fluoro group and a methoxy group make it a valuable tool in designing and synthesizing complex organic molecules. Specifically, 2-Fluoro-4-methoxyphenol is employed in the development of novel drug candidates, herbicides, and advanced materials. Its role in chemical synthesis extends to applications in medicinal chemistry, where it can be modified to enhance drug potency or selectivity. Furthermore, this compound is a valuable intermediate in the creation of specialty polymers and organic compounds used in diverse industries. With its diverse applications and utility in organic synthesis, 2-Fluoro-4-methoxyphenol plays a crucial role in advancing the field of chemistry and driving innovation in various sectors.