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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)-

1-pyridin-2-ylethanol

CC(c1ccccn1)O Request for Quotation
Chemical Name: 1-pyridin-2-ylethanol
CAS Number: 18728-61-5
Product Number: AG003EPF(AGN-PC-0JLWEI)
Synonyms:
MDL No: MFCD06245419
Molecular Formula: C7H9NO
Molecular Weight: 123.1525

Identification/Properties

Properties
MP:
53-54℃
BP:
210.6°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
123.155g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
123.068g/mol
Monoisotopic Mass:
123.068g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
85
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(Pyridin-2-yl)ethanol, also known as pyridine-2-ethanol or 2-pyridyl ethanol, is a versatile organic compound frequently used in chemical synthesis. This compound serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure, combining a pyridine ring with an ethanol group, confers specific reactivity and functionality that make it a popular choice in synthetic chemistry.In chemical synthesis, 1-(Pyridin-2-yl)ethanol can participate in a range of reactions, such as nucleophilic substitution, oxidation, and condensation reactions. Its pyridine moiety offers opportunities for further functionalization and diversification through various synthetic pathways. Additionally, the presence of the ethanol group allows for compatibility with aqueous and organic solvents, expanding its applicability in different reaction conditions.One common application of 1-(Pyridin-2-yl)ethanol is as a precursor for the synthesis of heterocyclic compounds, which are essential structural motifs in many bioactive molecules. By strategically incorporating this compound into synthetic routes, chemists can access a wide array of functionalized pyridine derivatives with tailored properties for specific applications in drug discovery, material science, and other fields of research.Overall, the utility of 1-(Pyridin-2-yl)ethanol in chemical synthesis lies in its ability to serve as a versatile intermediate for the construction of complex organic molecules with valuable biological or industrial applications. Through creative chemical transformations and strategic design, this compound contributes to the advancement of synthetic chemistry and the development of new functional materials.