ChemicalBook > Product Catalog > Pharmaceutical intermediates > Heterocyclic compound > Pyridine compound > Methylpyridine > 2,6-BIS(BROMOMETHYL)PYRIDINE
2,6-BIS(BROMOMETHYL)PYRIDINE
2,6-BIS(BROMOMETHYL)PYRIDINE Basic information
- Product Name:
- 2,6-BIS(BROMOMETHYL)PYRIDINE
- Synonyms:
-
- 2,6-Bis(broMoMethyl)pyridine 98%
- 2,6-Di(bromomethyl)pyridine
- alpha,alpha'-Dibromo-2,6-lutidine
- 2,6-BIS(BROMOMETHYL)PYRIDINE
- 2,6-Bis(bromomethyl)pyridine >
- Pyridine, 2,6-bis(bromomethyl)-
- 2,6-BIS(BROMOMETHYL)PYRIDINE ISO 9001:2015 REACH
- SKL650
- CAS:
- 7703-74-4
- MF:
- C7H7Br2N
- MW:
- 264.95
- Product Categories:
-
- C7 and C8Heterocyclic Building Blocks
- Halogenated Heterocycles
- Heterocyclic Building Blocks
- Pyridines
- Building Blocks
- C7 to C18
- C7 to C8
- Chemical Synthesis
- Halogenated Heterocycles
- Heterocyclic Building Blocks
- Mol File:
- 7703-74-4.mol
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2,6-BIS(BROMOMETHYL)PYRIDINE Chemical Properties
- Melting point:
- 85-87 °C(lit.)
- Boiling point:
- 275.6±30.0 °C(Predicted)
- Density
- 1.870±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- powder to crystaline
- pka
- 1.65±0.24(Predicted)
- color
- White to Almost white
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Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 22-36/37/38
- 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(BROMOMETHYL)PYRIDINE Usage And Synthesis
Uses
2,6-Bis(bromomethyl)pyridine may be used in the preparation of the following:
- a new pyridine-pyrazole derivative, 2,6-bis(3,5-diphenylpyrazol-1-ylmethyl)pyridine
- a large macrocyclic ligand, N(1),N(7)-pyridine-2,6-dimethyl-N(2),N(6)-bis(6-(3-(1H-benzo[d]imidazol-1-yl)propanamido)pyridin-2-yl)pyridine-2,6-dicarboxamide dibromide
- small-ring, potentially tridentate Se(2)N(pyridyl)-donor macrocycles
General Description
Crystal of 2,6-bis(bromomethyl)pyridine has the molecules related by a c-glide-plane operation. Molecules are arranged into stacks along the c axis. It participates in the synthesis of dicationic imidazolium-linked cyclophane.
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