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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, 3,5-dichloro-4-methyl-

Clc1cncc(c1C)Cl Request for Quotation
Chemical Name: Pyridine, 3,5-dichloro-4-methyl-
CAS Number: 100868-46-0
Product Number: AG00031O(AGN-PC-0NDF6F)
Synonyms:
MDL No:
Molecular Formula: C6H5Cl2N
Molecular Weight: 162.0166

Identification/Properties

Computed Properties
Molecular Weight:
162.013g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
160.98g/mol
Monoisotopic Mass:
160.98g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
9
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:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,5-Dichloro-4-Picoline, a versatile chemical compound, finds wide applications in various chemical synthesis processes. Primarily, it is utilized as a crucial building block in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique molecular structure and reactivity make it an essential intermediate in the synthesis of complex organic compounds.In pharmaceutical synthesis, 3,5-Dichloro-4-Picoline serves as a key starting material for the production of biologically active molecules such as antimalarial drugs, antiviral agents, and anti-inflammatory medications. Its chlorinated aromatic ring provides opportunities for introducing specific functional groups required for enhancing the pharmacological properties of the final drug molecules.Furthermore, in agrochemical applications, 3,5-Dichloro-4-Picoline plays a vital role in the development of crop protection chemicals like herbicides, fungicides, and insecticides. By incorporating this compound into the chemical synthesis processes, researchers can tailor the properties of these agrochemicals for improved efficiency and selectivity in targeting pests and diseases affecting crops.Additionally, in the realm of specialty chemicals, 3,5-Dichloro-4-Picoline acts as a valuable intermediate for the synthesis of various industrial chemicals and materials. Its versatile reactivity enables chemists to access a diverse range of derivatives that can be further functionalized for specific industrial applications, including the production of dyes, pigments, and coatings.Overall, the strategic use of 3,5-Dichloro-4-Picoline in chemical synthesis highlights its significance as a versatile building block for the efficient and targeted development of pharmaceuticals, agrochemicals, and specialty chemicals, offering valuable opportunities for advancing research and innovation in the field of organic chemistry.