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Thermo Scientific Chemicals
2,6-Dichloro-3-methylpyridine, 98%, Thermo Scientific Chemicals
| 製品番号（カタログ番号） | 数量 |
|---|---|
| H61271.03 または、製品番号H61271-03 | 1 g |
化学物質識別子
CAS58584-94-4
IUPAC Name2,6-dichloro-3-methylpyridine
Molecular FormulaC6H5Cl2N
InChI KeyKNIKCOPEHZTQJV-UHFFFAOYSA-N
SMILESCC1=C(Cl)N=C(Cl)C=C1
さらに表示
仕様
スペックシート
スペックシート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.
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:
- 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.
- 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.