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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-Quinolinol, 2-methyl-

Oc1cc2ccccc2nc1C Request for Quotation
Chemical Name: 3-Quinolinol, 2-methyl-
CAS Number: 613-19-4
Product Number: AG00EHDM(AGN-PC-0JTH3Z)
Synonyms:
MDL No:
Molecular Formula: C10H9NO
Molecular Weight: 159.1846

Identification/Properties

Computed Properties
Molecular Weight:
159.188g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
159.068g/mol
Monoisotopic Mass:
159.068g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
160
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


2-Methylquinolin-3-ol, also known as 2-Methyl-3-hydroxyquinoline, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in organic chemistry reactions due to its unique structure and reactivity. In particular, 2-Methylquinolin-3-ol is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.One key application of 2-Methylquinolin-3-ol is its role as a precursor in the synthesis of various pharmaceutical agents. This compound's hydroxyl group can undergo various chemical transformations, such as esterification or etherification, to introduce specific functional groups required for drug development. Furthermore, the quinoline ring structure of 2-Methylquinolin-3-ol provides a scaffold for the design and synthesis of bioactive molecules with diverse pharmacological properties.Additionally, 2-Methylquinolin-3-ol is utilized in the preparation of agrochemicals, including pesticides and herbicides. By incorporating this compound into the chemical structure of agricultural products, researchers can enhance their efficacy and specificity in targeting pests or weeds. The presence of the methyl group in 2-Methylquinolin-3-ol offers synthetic chemists the flexibility to modify the molecule further to optimize its biological activity.Moreover, 2-Methylquinolin-3-ol plays a crucial role in the synthesis of specialty chemicals used in various industrial applications. Its strategic placement of functional groups allows for the introduction of specific properties, such as solubility, stability, or reactivity, into the final product. This versatility makes 2-Methylquinolin-3-ol a valuable intermediate for the production of tailored chemical compounds with desired characteristics.Overall, the diverse applications of 2-Methylquinolin-3-ol in chemical synthesis highlight its importance as a key building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable tool for organic chemists seeking to create novel molecules with targeted properties and applications.