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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)-

(3-fluoro-5-methoxyphenyl)methanol

OCc1cc(OC)cc(c1)F Request for Quotation
Chemical Name: (3-fluoro-5-methoxyphenyl)methanol
CAS Number: 914637-27-7
Product Number: AG0039YR(AGN-PC-058CIH)
Synonyms:
MDL No:
Molecular Formula: C8H9FO2
Molecular Weight: 156.1543

Identification/Properties

Computed Properties
Molecular Weight:
156.156g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
156.059g/mol
Monoisotopic Mass:
156.059g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
119
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:
Danger
UN#:
2811
Hazard Statements:
H301
Precautionary Statements:
P301+P310
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The versatile compound (3-Fluoro-5-methoxyphenyl)methanol plays a crucial role in chemical synthesis as a key building block. With its unique molecular structure, this compound serves as a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and materials. Its strategic placement of functional groups allows for precise manipulation and integration into complex molecular frameworks. By serving as a starting point in synthetic pathways, (3-Fluoro-5-methoxyphenyl)methanol contributes to the creation of innovative compounds with diverse applications. Its importance lies in its ability to facilitate the synthesis of novel molecules with enhanced properties and functionalities, making it a valuable tool in the realm of organic chemistry and drug discovery.