3-Benzyloxybenzeneboronic acid

3-Benzyloxybenzeneboronic acid Basic information
Product Name:3-Benzyloxybenzeneboronic acid
Synonyms:AKOS BRN-0080;3-BENZYLOXYPHENYLBORONIC ACID;3-BENZYLOXYBENZENEBORONIC ACID;3-Benzyloxyphenylboronic;M-BENZYLOXYPHENYLBORONIC ACID;3-BENZYLOXYBENZENEBORONIC ACID, 98+%;3-BENZYLOXYPHENYBORONIC ACID;3-Benzyloxyphenylboronic Acid (contains varying amounts of Anhydride)
CAS:156682-54-1
MF:C13H13BO3
MW:228.05
EINECS:674-523-3
Product Categories:Boronate Ester;Potassium Trifluoroborate;Aryl Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Monosubstituted Aryl Boronic Acids;Organometallic Reagents;Boronic Acids;Boronic Acids and Derivatives;B (Classes of Boron Compounds);Boronic acids;Aryl;Boronic acid;Organoborons;BoronicAcids;blocks
Mol File:156682-54-1.mol
3-Benzyloxybenzeneboronic acid Structure
3-Benzyloxybenzeneboronic acid Chemical Properties
Melting point 125-130 °C (lit.)
Boiling point 428.2±47.0 °C(Predicted)
density 1.20±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
Water Solubility Slightly soluble in water
pka8.10±0.10(Predicted)
form Crystalline Powder or Crystals
color White to beige
BRN 6808244
CAS DataBase Reference156682-54-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,C
Risk Statements 36/37/38
Safety Statements 37/39-26-36-26/37
WGK Germany 3
Hazard Note Corrosive
HazardClass IRRITANT
HS Code 29310095
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
3-Benzyloxybenzeneboronic acid Usage And Synthesis
Chemical Propertieswhite crystalline powde
UsesReactant for:
  • Microwave Suzuki-Miyaura coupling
  • Preparation of palladium-based fluoride-derived electrophilic fluorination reagent for PET imaging agents
  • Synthesis of substituted isoindolines via palladium-catalyzed cascade reaction
  • Ruthenium-catalyzed hydrogenation
  • Suzuki coupling reactions
Usessuzuki reaction
UsesReactant for:• ;Microwave Suzuki-Miyaura coupling1• ;Preparation of palladium-based fluoride-derived electrophilic fluorination reagent for PET imaging agents2• ;Synthesis of substituted isoindolines via palladium-catalyzed cascade reaction3• ;Ruthenium-catalyzed hydrogenation4• ;Suzuki coupling reactions5
General DescriptionContains varying amounts of anhydride.
4-Tolylboronic acid 3-(3'-Chlorobenzyloxy)phenylboronic acid 4-Methoxybenzyl cyanide 3-BENZYLOXY-4-METHOXYBORONIC ACID, PINACOL ESTER 3-(3'-METHOXYBENZYLOXY)PHENYLBORONIC AC& Ethyl 2-(Chlorosulfonyl)acetate 2-(3-BENZYLOXYPHENYL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE 2,6-DIFLUORO-3-(2'-FLUOROBENZYLOXY)PHEN& 3-(2-FLUOROBENZYLOXY)PHENYLBORONIC ACID Ascoric Acid 2,6-DIFLUORO-3-(2'-CHLOROBENZYLOXY)PHEN& 4-BENZYLOXY-3-CHLOROPHENYLBORONIC ACID 3-(4'-CHLOROBENZYLOXY)PHENYLBORONIC ACID 3-(2'-CHLOROBENZYLOXY)PHENYLBORONIC ACID 2-BENZYLOXYBENZENEBORONIC ACID 2,6-DIFLUORO-3-(3',5'-DIMETHOXYBENZYLOX& 4-BENZYLOXYBENZENEBORONIC ACID, PINACOL ESTER,4-Benzyloxybenzeneboronic acid, pinacol ester 98% 3-(Benzyloxy)-2,6-difluorobenzeneboronic acid

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