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6-Bromopyridine-2-carbaldehyde

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6-Bromopyridine-2-carbaldehyde Basic information

Product Name:
6-Bromopyridine-2-carbaldehyde
Synonyms:
  • 6-BROMOPYRIDINE-2-CARBALDEHYDE
  • 6-BROMOPYRIDINE-2-CARBOXALDEHYDE
  • 6-BROMO-2-FORMYLPYRIDINE
  • 6-BROMO-2-PYRIDINE CARBOXALDEHYDE
  • 6-bromopyridine-2-barboxaldehyde
  • 2-BROMOPYRIDINE-6-CARBOXALDEHYDE
  • 2-BROMO-6-FORMYLPYRIDINE
  • 6-BROMO-PYRIDINE CARBOXALDEHYDE
CAS:
34160-40-2
MF:
C6H4BrNO
MW:
186.01
EINECS:
608-952-4
Product Categories:
  • Building Blocks
  • Pyridine Series
  • Aldehydes
  • Pyridines
  • Nucleotides and Nucleosides
  • Bases & Related Reagents
  • Pyridine
  • Nucleotides
  • C6Heterocyclic Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Heterocycle-Pyridine series
Mol File:
34160-40-2.mol
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6-Bromopyridine-2-carbaldehyde Chemical Properties

Melting point:
81-85 °C(lit.)
Boiling point:
248.2±20.0 °C(Predicted)
Density 
1.683±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
Chloroform (Sparingly), Dichloromethane, Ether, Ethyl Acetate, Methanol (Slightl
form 
Powder
pka
1.00±0.10(Predicted)
color 
White to beige or pale brown
Water Solubility 
Soluble in dichloromethane, ether, ethyl acetate and methanol. Insoluble in water.
Sensitive 
Air Sensitive
BRN 
1524300
InChIKey
QWFHFNGMCPMOCD-UHFFFAOYSA-N
CAS DataBase Reference
34160-40-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn,F
Risk Statements 
36/37/38-20/21/22-10
Safety Statements 
26-36-36/37/39-16
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29333990

MSDS

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6-Bromopyridine-2-carbaldehyde Usage And Synthesis

Chemical Properties

Light yellow Flakes

Uses

6-Bromopyridine-2-carboxaldehyde is used in the study of a rhodium-catalyzed, reductive aldol coupling with divinyl ketones leading to syn ?-hydroxyenones. It is also used as a building block for Tris[(pyridyl)methyl]amine ligands.

Uses

6-Bromopyridine-2-carbaldehyde can be a useful synthetic intermediate.

General Description

6-Bromo-2-pyridinecarboxaldehyde is a pyridine derivative. It participates in the synthesis of meso-substituted trans-A2B2-porphyrin.

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