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2-AMINO-3-FORMYLCHROMONE

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2-AMINO-3-FORMYLCHROMONE Basic information

Product Name:
2-AMINO-3-FORMYLCHROMONE
Synonyms:
  • 2-amino-4-oxo-chromene-3-carbaldehyde
  • 2-amino-4-oxochromene-3-carbaldehyde
  • 2-amino-4-keto-chromene-3-carbaldehyde
  • 2-amino-4-oxo-3-chromenecarboxaldehyde
  • 2-AMINO-3-FORMYLCHROMONE
  • 2-AMINO-4-OXO-4 H-1-BENZOPYRAN-3-CARBOXALDEHYDE
  • 2-AMINO-4-OXO-4H-CHROMENE-3-CARBALDEHYDE
  • 2-Aminochromone-3-carboxaldehyde
CAS:
61424-76-8
MF:
C10H7NO3
MW:
189.17
Product Categories:
  • Chromones
  • Heterocyclic Compounds
Mol File:
61424-76-8.mol
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2-AMINO-3-FORMYLCHROMONE Chemical Properties

Melting point:
249 °C (dec.) (lit.)
Boiling point:
401.2±45.0 °C(Predicted)
Density 
1.486±0.06 g/cm3(Predicted)
pka
1.31±0.20(Predicted)
form 
powder to crystal
color 
White to Orange to Green
CAS DataBase Reference
61424-76-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2932.99.9090
HazardClass 
IRRITANT

MSDS

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2-AMINO-3-FORMYLCHROMONE Usage And Synthesis

Uses

2-Amino-3-formylchromone may be used in the preparation of the following:

  • chiral Schiff base ligands (R)/(S)-2-amino-3-(((1-hydroxypropan-2-yl)imino)methyl)-4H-chromen-4-one
  • hydrazone derivatives, required for the synthesis of heterocyclic Schiff′s bases having antimicrobial activity
  • N-{4-[(6-chloro-4-oxo-4H-chromen-3-ylmethylene)amino]phenyl}-3,5-dimethyl-benzofuran-2-carboxamide
  • N-{4-[(6-chloro-4-oxo-4H-chromen-3-ylmethylene)amino]phenyl}-1,4-dihydro-chromono [2,3-b]pyrrole-2-carboxamide
  • 6-chloro-3-{[4-(2-thioxo-3,6-dihydro-2H-1,3,4-thiadiazin-5-ylamino)phenylimino] methyl}- 4-oxo-4H -chromene
  • 3--(2-amino--4--oxo--4H--chromen--3--yl)methylidene)--6-- ethyl--2H--pyrano[3,2--c]quinolone--2,4,5(3H,6H)-trione

General Description

2-Amino-3-formylchromone (2-Amino-4-oxo-4H-1-benzopyran-3-carboxaldehyde) is a benzopyran derivative. It is a bicyclic heterocyclic molecule made up of a benzene ring fused to a heterocyclic pyran ring. It undergoes condensation with (R)-2-amino-2-phenylethanol to afford Schiff base ligand, which forms complexes with Cu(NO3)2 and Zn(NO3)2.

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