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2,4-Dichlorophenylboronic acid

Basic information Safety Supplier Related

2,4-Dichlorophenylboronic acid Basic information

Product Name:
2,4-Dichlorophenylboronic acid
Synonyms:
  • Dichlorophenylboronic aci
  • 2,4-DICHLOROBENZENEBORONIC ACID
  • 2,4-DICHLOROPHENYLBORNIC ACID
  • 2,4-DICHLOROPHENYLBORONIC ACID
  • RARECHEM AH PB 0087
  • AKOS BRN-0144
  • 2,4-Dicholorophenylboronic acid
  • 2,4-Dichlorobenzeneboronicacid,98%
CAS:
68716-47-2
MF:
C6H5BCl2O2
MW:
190.82
Product Categories:
  • Aryl Boronic Acids
  • Boronic Acids and Derivatives
  • B (Classes of Boron Compounds)
  • Chemical Synthesis
  • Disubstituted Aryl Boronic Acids
  • Organometallic Reagents
  • Fluorin-contained phenyl boronic acid series
  • blocks
  • BoronicAcids
  • Boronic Acid series
  • Boronic acids
  • Boronic Acid
  • Aryl
  • Organoborons
Mol File:
68716-47-2.mol
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2,4-Dichlorophenylboronic acid Chemical Properties

Melting point:
246-249 °C (lit.)
Boiling point:
331.3±52.0 °C(Predicted)
Density 
1.47±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Methanol
pka
8.10±0.58(Predicted)
form 
Powder
color 
White to off-white
BRN 
4983878
CAS DataBase Reference
68716-47-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
36/37/38-22
Safety Statements 
37/39-26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29163990

MSDS

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2,4-Dichlorophenylboronic acid Usage And Synthesis

Chemical Properties

white to off-white powder

Uses

suzuki reaction

Uses

Reactant involved in:

  • Suzuki coupling reactions with alkynyl bromides or aniline / thiophenol
  • Selective hydroxylation to phenols

Reactant involved in synthesis of biologically active molecules including:
  • N-hydroxyindole-2-carboxylates for use as lactate dehydrogenase inhibitors
  • Non-ATP competitive MK2 inhibitors

Uses

2,4-Dichlorophenylboronic acid is used as reactant involved in:
• Suzuki coupling reactions with alkynyl bromides or aniline / thiophenol
• Selective hydroxylation to phenols4Reactant involved in synthesis of biologically active molecules including:
• N-hydroxyindole-2-carboxylates for use as lactate dehydrogenase inhibitors
• Non-ATP competitive MK2 inhibitors

2,4-Dichlorophenylboronic acidSupplier

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