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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, 3-fluoro-4-methyl-

OCc1ccc(c(c1)F)C Request for Quotation
Chemical Name: Benzenemethanol, 3-fluoro-4-methyl-
CAS Number: 192702-79-7
Product Number: AG002G8J(AGN-PC-0KKW9K)
Synonyms:
MDL No:
Molecular Formula: C8H9FO
Molecular Weight: 140.1549

Identification/Properties

Properties
MP:
33-36℃
Storage:
Room Temperature;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
140.157g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
140.064g/mol
Monoisotopic Mass:
140.064g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
105
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P264-P271-P302+P352-P305+P351+P338-P362-P403+P233-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (3-Fluoro-4-methylphenyl)methanol compound is commonly used as a versatile building block in chemical synthesis processes. Its unique molecular structure and functional groups make it a valuable intermediate in the production of various organic compounds.In organic synthesis, (3-Fluoro-4-methylphenyl)methanol can serve as a precursor for the preparation of complex molecules such as pharmaceuticals, agrochemicals, and materials. It can undergo reactions such as esterification, oxidation, or reduction to introduce different functional groups, thereby enabling the formation of diverse chemical products.Additionally, the presence of the fluoro and methyl groups in the molecule can impart specific properties to the final compounds synthesized from (3-Fluoro-4-methylphenyl)methanol. These properties may include enhanced biological activity, improved stability, or altered physical characteristics, depending on the intended application of the synthesized compounds.Overall, the strategic incorporation of (3-Fluoro-4-methylphenyl)methanol into chemical synthesis pathways can facilitate the efficient and tailored production of valuable organic molecules with a wide range of potential applications.