2,6-Dichloro-3-methylpyridine, 98%, Thermo Scientific Chemicals
2,6-Dichloro-3-methylpyridine, 98%, Thermo Scientific Chemicals
2,6-Dichloro-3-methylpyridine, 98%, Thermo Scientific Chemicals
2,6-Dichloro-3-methylpyridine, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2,6-Dichloro-3-methylpyridine, 98%, Thermo Scientific Chemicals

Catalog NumberQuantity
H61271.03
also known as H61271-03
1 g
Catalog number H61271.03
also known as H61271-03
Price (JPY)
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1 g
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Chemical Identifiers
CAS58584-94-4
IUPAC Name2,6-dichloro-3-methylpyridine
Molecular FormulaC6H5Cl2N
InChI KeyKNIKCOPEHZTQJV-UHFFFAOYSA-N
SMILESCC1=C(Cl)N=C(Cl)C=C1
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SpecificationsSpecification SheetSpecification Sheet
Assay (HPLC)>97.5%
2,6-Dichloro-3-methylpyridine is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2,6-Dichloro-3-methylpyridine is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.

Solubility
Slightly soluble in water.

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Taisuke Katoh.; Yoshihide Tomata.; Tetsuya Tsukamoto, Yoshihisa Nakada. Facile preparation of 3-substituted-2,6-difluoropyridines: application to the synthesis of 2,3,6-trisubstituted pyridines. Tetrahedron Letters. 2015, 56 (44), 6043-6046.
  2. Peter Bach.; Michaela Marczynke.; Fabrizio Giordanetto. Effects of the Pyridine 3-Substituent on Regioselectivity in the Nucleophilic Aromatic Substitution Reaction of 3-Substituted 2,6-Dichloropyridines with 1-Methylpiperazine Studied by a Chemical Design Strategy. European Journal of Organic Chemistry. 2012, 2012 (35), 6940-6952.