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2-Amino-3,5-dibromobenzaldehyde

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2-Amino-3,5-dibromobenzaldehyde Basic information

Product Name:
2-Amino-3,5-dibromobenzaldehyde
Synonyms:
  • 3,5-DIBROMOANTHRALDEHYDE
  • 3,5-DIBROMOANTHRANILALDEHYDE
  • 3,5-DIBROMANTHRANILALDEHYD
  • 2-AMINO-3,5-DIBROMOBENZALDEHYDE
  • 3,5-Dibromo-2-aminobenzaldehyde
  • 2-AMINO-3,5-DIBROMOBENZALDEHYDE 98+%
  • 2-Amino-3,5-Bromo Benzaldehyde
  • 2-AMINO-3,5-DIBROMOBENZALDEHYDE=3,5-DIBROMOANTHRANILALDEHYDE
CAS:
50910-55-9
MF:
C7H5Br2NO
MW:
278.93
EINECS:
256-841-0
Product Categories:
  • Aromatics, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
  • Aromatics
  • Benzaldehyde
  • Intermediates & Fine Chemicals
  • Metabolites & Impurities
  • Pharmaceuticals
  • Aromatic Aldehydes & Derivatives (substituted)
  • (intermediate of ambroxol hcl)
  • Ambroxol
  • Aldehydes
  • C7
  • Carbonyl Compounds
  • john's
  • 1
Mol File:
50910-55-9.mol
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2-Amino-3,5-dibromobenzaldehyde Chemical Properties

Melting point:
130-135 °C (lit.)
Boiling point:
319.9±42.0 °C(Predicted)
Density 
2.0123 (rough estimate)
refractive index 
1.6400 (estimate)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Solid
pka
-2.29±0.10(Predicted)
color 
Yellow
Sensitive 
Air Sensitive
InChIKey
RCPAZWISSAVDEA-UHFFFAOYSA-N
CAS DataBase Reference
50910-55-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-36
Safety Statements 
37/39-26-36
WGK Germany 
3
HS Code 
29223990

MSDS

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2-Amino-3,5-dibromobenzaldehyde Usage And Synthesis

Chemical Properties

Yellow crystalline powder

Uses

2-Amino-3,5-dibromobenzaldehyde may be employed in the preparation of tetradentate Schiff base ligands, via condensation with aliphatic diamines. These ligands forms nickel (II) and oxovanadium(IV) complexes.

Uses

2-Amino-3,5-dibromobenzaldehyde is a reagent used in the preparation of Ambroxol and Bromhexine (B678600) metabolites.

General Description

2-Amino-3,5-dibromobenzaldehyde has been identified as one of the oxidation product of bromhexine by controlled potential electrolysis followed by HPLC-UV and GC-MS. It participates in the Friedl?nder condensation of C-β?glycosylic ketones to form 2-substituted quinoline derivatives.

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