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2,4-DIMETHYLPHENYLBORONIC ACID

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2,4-DIMETHYLPHENYLBORONIC ACID Basic information

Product Name:
2,4-DIMETHYLPHENYLBORONIC ACID
Synonyms:
  • M-XYLENE-4-BORONIC ACID
  • AKOS BRN-0225
  • 2,4-Dimethylphenylboronic
  • 2,4-DIMETHYLPHENYLBORONIC ACID
  • 2,4-DIMETHYLBENZENEBORONIC ACID
  • 2,4-Dimethylphenylboronic Acid (contains varying amounts of Anhydride)
  • 2,4-Dimethylphenylboronic acid ,98%
  • 4-Borono-m-xylene
CAS:
55499-44-0
MF:
C8H11BO2
MW:
149.98
Product Categories:
  • Triazoles
  • B (Classes of Boron Compounds)
  • Boronic acid
  • Organoborons
  • blocks
  • BoronicAcids
  • Boronic acids
  • Aryl
Mol File:
55499-44-0.mol
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2,4-DIMETHYLPHENYLBORONIC ACID Chemical Properties

Melting point:
204-208°C
Boiling point:
292.4±50.0 °C(Predicted)
Density 
1.07±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
Water Solubility 
Slightly soluble in water
form 
powder to crystal
pka
8.92±0.58(Predicted)
color 
White to Light yellow
CAS DataBase Reference
55499-44-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-36/37/39-36/37-37
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29319090

MSDS

  • Language:English Provider:ALFA
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2,4-DIMETHYLPHENYLBORONIC ACID Usage And Synthesis

Chemical Properties

White powder

Uses

suzuki reaction

Synthesis

5419-55-6

583-70-0

55499-44-0

The general procedure for the synthesis of 2,4-dimethylphenylboronic acid from triisopropyl borate and 2,4-dimethylbromobenzene was as follows: 3.42 g (0.140 mol) of magnesium and 9 mL of tetrahydrofuran were added to a reaction vessel fitted with a dropping funnel under nitrogen protection. Subsequently, a solution consisting of 20.0 g (0.108 mol) of 2,4-dimethylbromobenzene dissolved in 60 mL of tetrahydrofuran (Eq. I-4-1) was added dropwise to prepare the Grignard reagent. After the reaction mixture was stirred for 2 hours, 14.6 g (0.140 mol) of trimethyl borate was added slowly and dropwise. After continued stirring for 2 hours, hydrochloric acid was added and stirred for 1 hour. Upon completion of the reaction, the organic layer was separated, washed with brine, and then the solvent was removed by distillation to afford 15.4 g (0.103 mol) of 2,4-dimethylphenylboronic acid (Formula I-4-2).

References

[1] Patent: JP2015/110532, 2015, A. Location in patent: Paragraph 0132-0133

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