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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, 4-(2-pyridinyl)-

OCc1ccc(cc1)c1ccccn1 Request for Quotation
Chemical Name: Benzenemethanol, 4-(2-pyridinyl)-
CAS Number: 98061-39-3
Product Number: AG0069XO(AGN-PC-0K6AHZ)
Synonyms:
MDL No:
Molecular Formula: C12H11NO
Molecular Weight: 185.2218

Identification/Properties

Properties
MP:
49 °C
BP:
353.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
185.226g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
185.084g/mol
Monoisotopic Mass:
185.084g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
164
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (4-(Pyridin-2-yl)phenyl)methanol plays a vital role in chemical synthesis as a versatile building block. With its unique structure containing both a pyridine and a phenyl group, this compound offers a wide range of synthetic possibilities. It can be utilized as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials.In organic synthesis, (4-(Pyridin-2-yl)phenyl)methanol can serve as a valuable starting material for the preparation of diverse molecules due to its ability to undergo various functional group transformations. Its functional groups can be modified through different reactions such as oxidation, reduction, and substitution, allowing for the introduction of new chemical moieties and the creation of structurally complex compounds.Additionally, the presence of the pyridine moiety in (4-(Pyridin-2-yl)phenyl)methanol imparts unique properties to the synthesized molecules, making them potentially useful in medicinal chemistry and material science. The pyridine ring can participate in coordination chemistry and impart specific biological activities to the final compounds, making it valuable in drug discovery and development.Overall, the utility of (4-(Pyridin-2-yl)phenyl)methanol in chemical synthesis lies in its versatility as a building block for the construction of diverse molecular structures with potential applications in pharmaceuticals, agrochemicals, and materials science.