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4-TERT-BUTYL-2,6-DIFORMYLPHENOL

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4-TERT-BUTYL-2,6-DIFORMYLPHENOL Basic information

Product Name:
4-TERT-BUTYL-2,6-DIFORMYLPHENOL
Synonyms:
  • 5-(tert-Butyl)-2-hydroxybenzene-1,3-dicarboxaldehyde, 4-(tert-Butyl)-2,6-diformylphenol
  • 5-(TERT-BUTYL)-2-HYDROXYISOPHTHALALDEHYDE
  • AKOS BC-1732
  • 4-TERT-BUTYL-2,6-DIFORMYLPHENOL
  • 5-(1,1-DIMETHYLETHYL)-2-HYDROXY-1,3-BENZENEDICARBOXALDEHYDE
  • 4-tert-Butyl-2,6-diforMylphenol 96%
  • 4-tert-Butyl-2,6-diformylphenol,5-(1,1-Dimethylethyl)-2-hydroxy-1,3-benzenedicarboxaldehyde
  • 4-tert-Butyl-2,6-diformylphenol
CAS:
84501-28-0
MF:
C12H14O3
MW:
206.24
Product Categories:
  • Aldehydes
  • Building Blocks
  • C10-C12
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
Mol File:
84501-28-0.mol
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4-TERT-BUTYL-2,6-DIFORMYLPHENOL Chemical Properties

Melting point:
99-103 °C(lit.)
Boiling point:
267.8±40.0 °C(Predicted)
Density 
1.159±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder
pka
6.61±0.23(Predicted)
color 
yellow
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2912490090

MSDS

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4-TERT-BUTYL-2,6-DIFORMYLPHENOL Usage And Synthesis

Uses

1. Used as a key intermediate for the production of a BODIPY chemodosimetric sensor for cyanide ions. 2. Used as a key intermediate for a Pro-ligand in bimetallic catalysis.

General Description

4-tert-Butyl-2,6-diformylphenol can be prepared from 4-tert-butylphenol and hexamethylenetetramine.

Synthesis

2203-14-7

84501-28-0

The general procedure for the synthesis of 4-tert-butyl-2,6-formylphenol from (5-(tert-butyl)-2-hydroxy-1,3-phenyl)dimethanol was as follows: activated MnO2 (40 g) was added to CHCl3 (200 mL) in a 500 mL round-bottom flask. The mixture was heated under stirring to reflux for about 15 minutes, then powder of (5-(tert-butyl)-2-hydroxy-1,3-phenyl)dimethanol (5.0 g) was added slowly. After keeping the reaction at reflux for 8 hours, the reaction mixture was cooled to room temperature and filtered through a Brinell funnel. The solid residue was washed thoroughly with CHCl3 (40 mL x 5) until the filtrate was colorless. The filtrates were combined and concentrated using a rotary evaporator to give the yellow solid product 4-tert-butyl-2,6-formylphenol (3.8 g, 77% yield).

References

[1] Synthetic Communications, 2000, vol. 30, # 9, p. 1555 - 1561
[2] Tetrahedron Letters, 2012, vol. 53, # 7, p. 804 - 807
[3] Bulletin of the Chemical Society of Japan, 1984, vol. 57, # 9, p. 2683 - 2684
[4] Chemische Berichte, 1994, vol. 127, # 3, p. 465 - 476
[5] Chemische Berichte, 1942, vol. 75, p. 363,366

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