2,4-Dichlorophenylboronic acid

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
EINECS:
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
2,4-Dichlorophenylboronic acid Structure
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
pka8.10±0.58(Predicted)
form Powder
color White to off-white
BRN 4983878
CAS DataBase Reference68716-47-2(CAS DataBase Reference)
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 Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
2,4-Dichlorophenylboronic acid Usage And Synthesis
Chemical Propertieswhite to off-white powder
Uses2,4-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



Usessuzuki reaction
UsesReactant 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
2,4-Dichlorophenylboronic acid Preparation Products And Raw materials
Preparation Products2,4-DICHLOROBIPHENYL-->4-Pyridinecarbonitrile, 2-amino-5-(2,4-dichlorophenyl)-
2,4-DICHLORO-3-METHOXYPHENYLBORONIC ACID 4-Chlorophenylboronic acid 2,3,4-Trichloro-5-nitrophenylboronic acid Phenylboronic acid 2,4-Dichloro-3-cyanophenylboronic acid p-Dichlorobenzene 2,4,6-Trichlorophenylboronic acid 3-(Benzyloxy)-2,4-dichlorophenylboronic acid 2,3,4-Trichlorophenylboronic acid 3,5-DICHLOROPHENYLBORONIC ACID, PINACOL ESTER Permethrin 2,4-Dichlorophenylboronic acid 1,3-Dichlorobenzene 2,4-DICHLORO-5-NITROPHENYLBORONIC ACID 2,4-DICHLOROPHENYLBORONIC ACID, PINACOL ESTER 2,4-Dichlorobenzyl chloride 1,2-Dichlorobenzene 2,4,5-Trichlorophenylboronic acid

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