4-Benzyloxybenzeneboronic acid

4-Benzyloxybenzeneboronic acid Basic information
Product Name:4-Benzyloxybenzeneboronic acid
Synonyms:RARECHEM AH PB 0041;P-BENZYLOXYPHENYLBORONIC ACID;AKOS BRN-0054;4-BENZYLOXYPHENYLBORONIC ACID;4-BENZYLOXYBENZENEBORONIC ACID;4-Benzyloxyphenylboronic;4-BEZYLOXYPHENYLBORONICACID;4-BENZYLOXYPHENYBORONIC ACID
CAS:146631-00-7
MF:C13H13BO3
MW:228.05
EINECS:678-070-2
Product Categories:Boronate Ester;Potassium Trifluoroborate;Boronic acids;B (Classes of Boron Compounds);Boronic Acids;Boronic Acids and Derivatives;Heterocyclic Compounds;Aryl;Boronic acid;Organoborons;blocks;BoronicAcids
Mol File:146631-00-7.mol
4-Benzyloxybenzeneboronic acid Structure
4-Benzyloxybenzeneboronic acid Chemical Properties
Melting point 193-199 °C
Boiling point 418.9±47.0 °C(Predicted)
density 1.20±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform, DMSO, Methanol
pka8.70±0.16(Predicted)
form solid
color White to Off-White
CAS DataBase Reference146631-00-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,C
Risk Statements 36/37/38
Safety Statements 37/39-26-36-24/25
WGK Germany 3
Hazard Note Corrosive
HazardClass IRRITANT
HS Code 29310095
MSDS Information
ProviderLanguage
ACROS English
ALFA English
4-Benzyloxybenzeneboronic acid Usage And Synthesis
Chemical Propertieswhite crystalline powder
Uses4-Benzyloxybenzeneboronic Acid is a reagent in the synthesis of arylalkenylpropargylamines as neuroprotective and potent selective monoamine oxidase B inhibitors. Also used to prepare pyridone alkaloids used as antiproliferative agents.
UsesIt is used as electronic intermediate. It is also utilized in HPLC and NMR spectroscopy.
Usessuzuki reaction
General DescriptionMay contain varying amounts of anhydride
4-Benzyloxybenzeneboronic acid Preparation Products And Raw materials
Raw materialsDiethyl ether-->Tetrahydrofuran-->Acetone-->n-Butyllithium-->Pentane-->Trimethyl borate-->Benzyl bromide-->4-Bromophenol
Preparation Products4-BENZYLOXYFLUOROBENZENE-->Ibrutinib D5-->METHYL 4'-(BENZYLOXY)[1,1'-BIPHENYL]-2-CARBOXYLATE
4-BENZYLOXY-3-CHLORO-5-METHYLPHENYLBORONIC ACID 4-Benzyloxy-2-formylphenylboronic acid 7-BENZYLOXYINDOLE-3-CARBOXYLIC ACID 4-(3'-CHLOROBENZYLOXY)-3,5-DIMETHYLPHEN& (2-(benzyloxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)(pyrrolidin-1-yl)methanone 4-(BENZYLOXY)-3,5-DICHLOROPHENYLBORONIC ACID 4-(4'-CHLOROBENZYLOXY)-3,5-DIMETHYLPHEN& 4-Benzyloxy-2-methylphenylboronic acid 3-CHLORO-4-(3'-BROMOBENZYLOXY)PHENYLBOR& 4-BENZYLOXY-3-CHLOROPHENYLBORONIC ACID 7-(BENZYLOXY)-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-INDOLE 3-CHLORO-4-(3'-CHLOROBENZYLOXY)PHENYLBO& 3-CHLORO-4-(4'-FLUOROBENZYLOXY)PHENYLBO& 4-(3,5-dimethoxybenzyloxy)phenylboronic acid 4-Benzyloxy-3-methylbenzeneboronic acid 3-CHLORO-4-(3',5'-DIMETHOXYBENXYLOXY)PH& 4-Benzyloxy-3,5-dimethylphenylboronic acid 4-(2'-CHLOROBENZYLOXY)-3,5-DIMETHYLPHEN&

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