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2-Methoxycarbonylphenylboronic acid

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2-Methoxycarbonylphenylboronic acid Basic information

Product Name:
2-Methoxycarbonylphenylboronic acid
Synonyms:
  • METHYL 2-BORONOBENZOATE
  • 2-(METHOXYCARBONYL)BENZENEBORONIC ACID
  • 2-METHOXYCARBONYLPHENYLBORONIC ACID
  • O-(METHOXYCARBONYL)PHENYLBORONIC ACID
  • Benzoic acid, 2-borono-, 1-methyl ester (9CI)
  • 2-Carbomethoxybenzeneboronicacid
  • 2-(Methoxycarbonyl)Phenylboron
  • 2-(Methoxycarbonyl)phenylboronic Acid (contains varying amounts of Anhydride)
CAS:
374538-03-1
MF:
C8H9BO4
MW:
179.97
Product Categories:
  • Aryl Boronic Acids
  • Boronic Acids and Derivatives
  • Chemical Synthesis
  • Monosubstituted Aryl Boronic Acids
  • Organometallic Reagents
  • Boronate Ester
  • Boronic Acid
  • Potassium Trifluoroborate
  • blocks
  • BoronicAcids
  • Carboxes
  • Boronic acids
  • BORONICACID
  • B (Classes of Boron Compounds)
  • Aryl
  • Boronic Acids
  • Boronic Acids and Derivatives
Mol File:
374538-03-1.mol
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2-Methoxycarbonylphenylboronic acid Chemical Properties

Melting point:
90-96°C
Boiling point:
359.0±44.0 °C(Predicted)
Density 
1.25±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
soluble in Methanol
pka
8.19±0.58(Predicted)
form 
Crystalline Powder
color 
White
BRN 
8313459
CAS DataBase Reference
374538-03-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
WGK Germany 
3
TSCA 
No
HazardClass 
IRRITANT
HS Code 
29163990

MSDS

  • Language:English Provider:ALFA
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2-Methoxycarbonylphenylboronic acid Usage And Synthesis

Chemical Properties

White to brown powder

Uses

2-Methoxycarbonylphenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

General Description

May contain varying amounts of anhydride

Synthesis

67-56-1

149105-19-1

374538-03-1

In a 20 L autoclave, 7.5 g of anhydrous methanol and 1.66 Kg (10 mol) of 2-carboxyphenylboronic acid were added and stirring was initiated to mix the reactants. The temperature of the reaction kettle was slowly raised to 40 °C and maintained in the range of 40 to 55 °C. Subsequently, thionyl chloride (1.31 Kg, 11 mol) was slowly added dropwise to the reaction kettle, and after the dropwise addition was completed, the temperature was raised to reflux condition and the reaction was continued for 2-3 hours. The completion of the reaction was confirmed by thin layer chromatography (TLC, unfolding agent ratio of n-heptane: ethyl acetate = 2:1). Upon completion of the reaction, the reaction solution was cooled and subsequently subjected to reduced pressure distillation to remove the solvent. The residue was cooled to -10°C to 10°C and stirred at this temperature for 1 hour. Next, the drying process was stopped by filtration under reduced pressure at 80 °C until no impurities were confirmed to be present by hydrogen nuclear magnetic resonance (HNMR, observing the peak at 3.21 ppm with DMSO-d6 as solvent). Finally, the mixture was stirred at room temperature, filtered and dried at room temperature to give 1.74 Kg of the white solid product 2-(methoxycarbonyl)phenylboronic acid in 96.7% yield with 19.8% water and 140.5% Karl Fischer moisture.

References

[1] Patent: CN106188117, 2016, A. Location in patent: Paragraph 0014

2-Methoxycarbonylphenylboronic acid Preparation Products And Raw materials

Raw materials

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