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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, 6-chloro-2,3-bis(chloromethyl)-

ClCc1nc(Cl)ccc1CCl Request for Quotation
Chemical Name: Pyridine, 6-chloro-2,3-bis(chloromethyl)-
CAS Number: 220001-94-5
Product Number: AG00CG7J(AGN-PC-005BRN)
Synonyms:
MDL No:
Molecular Formula: C7H6Cl3N
Molecular Weight: 210.48824

Identification/Properties

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


6-Chloro-2,3-bis(chloromethyl)pyridine is a versatile compound widely used in chemical synthesis as a key building block for the creation of various organic molecules. Its unique structure consists of a pyridine ring with chloromethyl groups attached at positions 2 and 3, along with an additional chlorine atom at position 6. One of the primary applications of 6-Chloro-2,3-bis(chloromethyl)pyridine is in the synthesis of complex organic compounds such as pharmaceuticals, agrochemicals, and specialty chemicals. The presence of multiple reactive sites on the molecule makes it a valuable intermediate for introducing functional groups or creating new carbon-carbon or carbon-nitrogen bonds in the desired target molecules.In organic synthesis, this compound can participate in various reactions like nucleophilic substitution, palladium-catalyzed cross-coupling reactions, and metal-catalyzed coupling reactions to form more intricate structures. Its reactivity and versatility make it a valuable tool for chemists seeking to design and create novel compounds with specific properties or functionalities.