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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)-

Pyridine, 4-chloro-2-(chloromethyl)-, hydrochloride

ClCc1nccc(c1)Cl.Cl Request for Quotation
Chemical Name: Pyridine, 4-chloro-2-(chloromethyl)-, hydrochloride
CAS Number: 119396-04-2
Product Number: AG000IOL(AGN-PC-03TWXG)
Synonyms:
MDL No:
Molecular Formula: C6H6Cl3N
Molecular Weight: 198.4775

Identification/Properties

Computed Properties
Molecular Weight:
198.471g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
196.957g/mol
Monoisotopic Mass:
196.957g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
87.1
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


4-Chloro-2-(chloromethyl)pyridine hydrochloride is a versatile compound commonly used in chemical synthesis as a key building block for various organic reactions. With its unique structure and reactivity, this compound serves as a valuable intermediate in the preparation of a wide range of pharmaceuticals, agrochemicals, and specialty chemicals.In organic synthesis, 4-Chloro-2-(chloromethyl)pyridine hydrochloride can undergo nucleophilic substitution reactions to introduce important functional groups into organic molecules. Its chloromethyl and chloro substituents provide opportunities for further derivatization, allowing chemists to tailor the compound for specific applications. This compound is particularly useful in the synthesis of bioactive compounds and intermediates for complex organic reactions.Furthermore, 4-Chloro-2-(chloromethyl)pyridine hydrochloride can be utilized in the preparation of heterocyclic compounds, which are essential building blocks in medicinal chemistry and materials science. Its ability to participate in diverse chemical transformations makes it a valuable tool for synthetic chemists seeking to create novel molecules with unique properties.In summary, the application of 4-Chloro-2-(chloromethyl)pyridine hydrochloride in chemical synthesis is crucial for the development of innovative compounds with potential implications in pharmaceuticals, agrochemicals, and other industries. Its versatility and reactivity make it an indispensable component in the toolkit of organic chemists striving to push the boundaries of chemical innovation.