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ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Phenols >  2,4,6-Triformylphloroglucinol

2,4,6-Triformylphloroglucinol

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2,4,6-Triformylphloroglucinol Basic information

Product Name:
2,4,6-Triformylphloroglucinol
Synonyms:
  • 2,4,6-trihydroxybenzene-1,3,5-tricarbaldehyde
  • 1,3,5-Benzenetricarboxaldehyde, 2,4,6-trihydroxy-
  • 2,4,6-Trihydroxy-1,3,5-benzenetricarbaldehyde, 95%
  • 2,4,6-Triformylphloroglucinol
  • triformylPhloroglucinol
  • Phloroglucinol Impurity 20
  • JACS-34374-88-4
  • Trialdehyde Resorcinol
CAS:
34374-88-4
MF:
C9H6O6
MW:
210.14
Product Categories:
  • COF
Mol File:
34374-88-4.mol
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2,4,6-Triformylphloroglucinol Chemical Properties

Melting point:
198-200 °C
Boiling point:
233.8±40.0 °C(Predicted)
Density 
1.755±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
DMSO (Slightly, Heated)
form 
Solid
pka
3.32±0.33(Predicted)
color 
Pale Orange
InChI
InChI=1S/C9H6O6/c10-1-4-7(13)5(2-11)9(15)6(3-12)8(4)14/h1-3,13-15H
InChIKey
KAPNIDMXEKQLMQ-UHFFFAOYSA-N
SMILES
C1(C=O)=C(O)C(C=O)=C(O)C(C=O)=C1O
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Safety Information

HS Code 
2912.49.6000
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2,4,6-Triformylphloroglucinol Usage And Synthesis

Uses

MOP is a phenolic organic compound which can be used as intermediate of synthetic materials.

Description

2,4,6-Triformylphloroglucinol (MOP)is a highly functionalised and symmetrical building block.

Physical properties

Pale orange solid

Uses

2,4,6-Triformylphloroglucinol is a chemical reagent used in gelation landscape engineering with a hydrogelator system to control products. This prevents the formation of hydrogel materials with vastly different properties. In addition, it is used in the preparation of luminescent nanoporous hybrid material to be used as a drug delivery system for anti-cancer agents.

Definition

2,4,6-Triformylphloroglucinol is a highly functionalised and symmetrical building block. 2,4,6-Triformylphloroglucinol contains 3 aldehyde groups which can react with nucleophiles, such as amines or anilines, to make β-ketoenamines. When the nucleophile contains more than one amine group, microporous polymers can be formed. These microporous polymers find a wide range of applications, including carbon dioxide capture.

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