1,4-Benzodioxane-6-boronic acid

1,4-Benzodioxane-6-boronic acid
  • CAS No.:164014-95-3
Other grades of this product :
1,4-Benzodioxane-6-boronic acid Basic information
Product Name:1,4-Benzodioxane-6-boronic acid
Synonyms:1,4-Benzodioxane-6-boronic acid ,97%;(1,4-BENZODIOXAN-6-YL)BORONIC ACID;1,4-BENZODIOXANE-6-BORONIC ACID;2,3-DIHYDROBENZO[B][1,4]DIOXIN-6-YLBORONIC ACID;2,3-DIHYDRO-1,4-BENZODIOXIN-6-YLBORONIC ACID;3,4-(ETHYLENEDIOXY)BENZENEBORONIC ACID;1,4-benzodioxan-6-boronic acid;2,3-Dihydro-1,4-benzodioxine-6-boronic acid
CAS:164014-95-3
MF:C8H9BO4
MW:179.97
EINECS:625-755-9
Product Categories:Boronic acids;Alkoxy;Aryl;Organoborons
Mol File:164014-95-3.mol
1,4-Benzodioxane-6-boronic acid Chemical Properties
Melting point 187 °C
Boiling point 361.0±52.0 °C(Predicted)
density 1.35±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
pka8.52±0.20(Predicted)
form powder
color white to off-white
BRN 7478648
CAS DataBase Reference164014-95-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37-37/39
WGK Germany 3
TSCA No
HazardClass IRRITANT
HS Code 29163990
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
1,4-Benzodioxane-6-boronic acid Usage And Synthesis
Chemical PropertiesWhite to light yellow crystal powder
UsesReactant involved in:
  • Addition reactions with 1,8-naphthyridine N-oxides
  • Iodocyclization and palladium-catalyzed coupling reactions for synthesis of pyranoquinolines
  • Suzuki coupling reactions for synthesis of combretastatin analogs
  • Suzuki-Miyaura coupling reactions for synthesis of aryl-substituted oxabenzindoles and methanobenzindoles
  • Palladium-catalyzed oxyarylation of Heck reaction intermediates
  • C-H functionalization of quinones
1,4-Benzodioxane-6-boronic acid Preparation Products And Raw materials
Raw materialsTetrahydrofuran-->Acetic acid-->Government regulation-->n-Butyllithium-->Triisopropyl borate-->1,4-Benzodioxan

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