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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-(chloromethyl)-6-methyl-, hydrochloride

ClCc1nc(C)ccc1O.Cl Request for Quotation
Chemical Name: 3-Pyridinol, 2-(chloromethyl)-6-methyl-, hydrochloride
CAS Number: 98280-34-3
Product Number: AG005VH3(AGN-PC-0J0Y17)
Synonyms:
MDL No:
Molecular Formula: C7H9Cl2NO
Molecular Weight: 194.0585

Identification/Properties

Properties
Storage:
2-8℃;Inert atmosphere;
Computed Properties
Molecular Weight:
194.055g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
193.006g/mol
Monoisotopic Mass:
193.006g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
110
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

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 2-(Chloromethyl)-6-methylpyridin-3-ol hydrochloride is a versatile compound widely used in chemical synthesis processes. Its unique structure allows it to participate in various reactions, making it a valuable building block for the synthesis of diverse organic molecules. In organic synthesis, this compound can serve as a key intermediate for the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, its chloromethyl and hydroxyl functionalities provide opportunities for further derivatization, enabling the synthesis of more complex molecules with specific properties and functions. Its hydrochloride salt form enhances its solubility and stability, facilitating its use in a wide range of synthetic applications.