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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, 2,6-dichloro-3-(chloromethyl)-

ClCc1ccc(nc1Cl)Cl Request for Quotation
Chemical Name: Pyridine, 2,6-dichloro-3-(chloromethyl)-
CAS Number: 41789-37-1
Product Number: AG00BY4T(AGN-PC-0WAJNK)
Synonyms:
MDL No:
Molecular Formula: C6H4Cl3N
Molecular Weight: 196.4617

Identification/Properties

Properties
MP:
89-90 °C
BP:
285.5 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
196.455g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
194.941g/mol
Monoisotopic Mass:
194.941g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
109
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,6-Dichloro-3-(chloromethyl)pyridine is a versatile chemical compound commonly used in chemical synthesis processes. This compound is valued for its ability to act as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals.One of the primary applications of 2,6-Dichloro-3-(chloromethyl)pyridine in chemical synthesis is in the preparation of heterocyclic compounds. By incorporating this compound into reactions, chemists are able to introduce specific functional groups and structural motifs into organic molecules, allowing for the development of new compounds with desired properties.Furthermore, 2,6-Dichloro-3-(chloromethyl)pyridine serves as an important intermediate in the synthesis of pyridine derivatives, which are widely used in medicinal chemistry and material science. Its unique chemical structure enables it to participate in a variety of transformations, leading to the synthesis of diverse molecules with potential applications in various industries.Overall, the strategic incorporation of 2,6-Dichloro-3-(chloromethyl)pyridine in chemical synthesis enables researchers to access a wide range of structurally complex and functionally diverse compounds, making it an indispensable tool in modern organic chemistry.