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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-Pyridinol, 2-ethyl-6-methyl-, hydrochloride

CCc1nc(C)ccc1O.Cl Request for Quotation
Chemical Name: 3-Pyridinol, 2-ethyl-6-methyl-, hydrochloride
CAS Number: 13258-59-8
Product Number: AG0010VR(AGN-PC-0JMLIG)
Synonyms:
MDL No:
Molecular Formula: C8H12ClNO
Molecular Weight: 173.6400

Identification/Properties

Computed Properties
Molecular Weight:
173.64g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
173.061g/mol
Monoisotopic Mass:
173.061g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
11
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Ethyl-6-methylpyridin-3-ol hydrochloride, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is widely utilized in various synthetic pathways to introduce unique functional groups and structural motifs into organic molecules. Its ability to undergo diverse chemical reactions makes it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. $name$ is especially prized for its compatibility with a range of reagents and catalysts, allowing for efficient and selective transformations in complex molecular designs. Its presence in the toolkit of organic chemists enables the construction of novel molecular architectures with tailored properties and functionalities. By leveraging the distinctive properties of 2-Ethyl-6-methylpyridin-3-ol hydrochloride, researchers can explore new avenues in drug discovery, materials science, and chemical engineering.