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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, 5-fluoro-2-methoxy-

COc1ccc(cc1O)F Request for Quotation
Chemical Name: Phenol, 5-fluoro-2-methoxy-
CAS Number: 72955-97-6
Product Number: AG003MQX(AGN-PC-0KKW8R)
Synonyms:
MDL No: MFCD00143459
Molecular Formula: C7H7FO2
Molecular Weight: 142.1277

Identification/Properties

Properties
BP:
223°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
142.129g/mol
XLogP3:
1.6
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoro-2-methoxyphenol, also known as FMOP, is a versatile compound widely used in chemical synthesis for its unique reactivity and properties. One of the key applications of 5-Fluoro-2-methoxyphenol in chemical synthesis is as a building block in the creation of pharmaceuticals and agrochemicals. Its fluoro and methoxy substituents provide opportunities for selective chemical reactions, making it a valuable intermediate in the synthesis of various bioactive compounds. Additionally, 5-Fluoro-2-methoxyphenol serves as a precursor in the preparation of specialty chemicals, including dyes, fragrances, and polymer additives. Its presence in synthetic pathways can impart specific functionalities and enhance the properties of the final product. In summary, the strategic incorporation of 5-Fluoro-2-methoxyphenol in chemical synthesis enables the efficient and controlled assembly of complex molecules with diverse applications.