ChemicalBook > Product Catalog > Pharmaceutical intermediates > Heterocyclic compound > Pyridine compound > Pyridine derivatives > 2,6-BIS(CHLOROMETHYL)PYRIDINE
2,6-BIS(CHLOROMETHYL)PYRIDINE
2,6-BIS(CHLOROMETHYL)PYRIDINE Basic information
- Product Name:
- 2,6-BIS(CHLOROMETHYL)PYRIDINE
- Synonyms:
-
- ALPHA,ALPHA'-DICHLORO-2,6-LUTIDINE
- α,α'-dichloro-2,6-lutidine
- 2,6-BIS(CHLOROMETHYL)PYRIDINE 98+%
- 2,6-Bis(chloromethyl)pyridine 99%
- 2,6-Bis(chloromethyl)pyridine,α,α′-Dichloro-2,6-lutidine
- 2,6-Bis(chloromethyl)pyridine >
- Pyridine, 2,6-bis(chloromethyl)-
- CAS:
- 3099-28-3
- MF:
- C7H7Cl2N
- MW:
- 176.04
- Product Categories:
-
- Pyridine
- Mol File:
- 3099-28-3.mol
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2,6-BIS(CHLOROMETHYL)PYRIDINE Chemical Properties
- Melting point:
- 73-78 °C (lit.)
- Boiling point:
- 110 °C / 3mmHg
- Density
- 1.275±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- powder to crystal
- pka
- 2.19±0.24(Predicted)
- color
- White to Almost white
- BRN
- 116355
- CAS DataBase Reference
- 3099-28-3(CAS DataBase Reference)
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Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 22-37/38-41
- Safety Statements
- 26-36/37/39
- RIDADR
- UN 3335
- WGK Germany
- 3
- HS Code
- 29333990
MSDS
- Language:English Provider:SigmaAldrich
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2,6-BIS(CHLOROMETHYL)PYRIDINE Usage And Synthesis
Chemical Properties
White to light yellow crystal powder
Uses
2,6-Bis(chloromethyl)pyridine may be used in the following studies:
- Synthesis of a sensitive fluorescent chemosensor for Hg2+, composed of two aminonaphthalimide fluorophores and a receptor of 2,6-bis(aminomethyl)pyridine.
- Preparation of carbene pincer ligands, required for the preparation of palladium pincer carbene complex.
- Synthesis of 2-(di-tert-butylphosphinomethyl)-6-diethylaminomethyl)pyridine, PNN ligand.
General Description
2,6-Bis(chloromethyl)pyridine is a heterocyclic building block for the synthesis of a variety of pyridine derivatives. It coordinates with metal ions through N-atom to form complexes. The conformational flexibility of the bromomethyl arms makes it an ideal choice for the generation of macrocycles. 2,6-bis(chloromethyl)pyridine crystals are monoclinic with space group P21/c. Its synthesis has been reported. The FT-IR and FT-Raman spectra of 2,6-bis(chloromethyl)pyridine (BCMP) have been recorded in the regions 4000-400cm-1 and 3500-100cm-1, respectively.
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