ChemicalBook Product Catalog Chemical Reagents Organic reagents Boric acid 4-Methoxyphenylboronic acid

4-Methoxyphenylboronic acid

4-Methoxyphenylboronic acid Basic information
Product Name:4-Methoxyphenylboronic acid
Synonyms:(4-methoxyphenyl)-boronicaci;p-methoxy-benzeneboronicaci;p-methoxyphenyl-boronicaci;RARECHEM AH PB 0191;TIMTEC-BB SBB004055;4-METHOXYPHENYLBORONIC ACID;4-Methoxyphenylboronic acid, 97% 1GR;(4-Methoxyphenyl)boric acid
CAS:5720-07-0
MF:C7H9BO3
MW:151.96
EINECS:611-482-2
Product Categories:Heterocyclic Compounds;Boronic Acid;Substituted Boronic Acids;Boronic acids;Alkoxy;Aryl;Organoborons;B (Classes of Boron Compounds);organic or inorganic borate;Aromatics;Intermediates;Miscellaneous Reagents;blocks;BoronicAcids;Boronic Acid series;Morpholines/Thiomorpholines ,Isoxazoles ,Indazoles;Boron Derivatives;Boronate Ester;Potassium Trifluoroborate;Aryl Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Monosubstituted Aryl Boronic Acids;Organometallic Reagents
Mol File:5720-07-0.mol
4-Methoxyphenylboronic acid Structure
4-Methoxyphenylboronic acid Chemical Properties
Melting point 204-206 °C(lit.)
Boiling point 306.8±44.0 °C(Predicted)
density 1.17±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Soluble in dimethyl sulfoxide and methanol.
form Crystalline Powder
pka8.96±0.10(Predicted)
color White to light beige
BRN 2936912
CAS DataBase Reference5720-07-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
RTECS CY8975000
TSCA No
HazardClass IRRITANT
HS Code 29310095
MSDS Information
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4-Methoxyphenylboronic acid English
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4-Methoxyphenylboronic acid Usage And Synthesis
Chemical Propertieswhite to light beige crystalline powder
Uses4-Methoxyphenylboronic acid can be used as a common organic reagent in Suzuki coupling reactions to study the N-arylation of imidazoles and amines catalyzed by copper exchange of calcium fluorophosphates.Reagent used in the preparation of various biological inhibitors.
Uses4-Methoxyphenylboronic acid is a reagent used for
Suzuki-Miyaura cross-coupling reactions
Pd-catalyzed direct arylation
Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water
Palladium-catalyzed stereoselective Heck-type reaction
Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence
Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides
Ruthenium catalyzed direct arylation
Rh-catalyzed asymmetric conjugate addition
Usessuzuki reaction
Uses4-Methoxylphenylboronic Acid is a phenylboronic acid used to investigate boron function in plants.
4-Methoxyphenylboronic acid Preparation Products And Raw materials
Preparation Products6-(4-METHOXYPHENYL)PYRIDINE-2-CARBALDEHYDE-->4-Nitroanisole-->4-Hydroxyphenylboronic acid-->4-Methoxyphenol-->4-BROMO-4'-METHOXYBENZOPHENONE-->3,5-DIIODOTHYROACETIC ACID-->4-Bromo-4'-methoxybiphenyl-->4,4'-Dimethoxybiphenyl-->1-(4-METHOXYPHENYL)-1H-IMIDAZOLE-->ETHYL 4-METHOXYPHENYLACETATE-->2-(4-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane-->4,4'-DIMETHOXYBENZHYDROL-->2-METHOXY-9H-CARBAZOLE-->4-Methoxybiphenyl
4-Aminophenylboronic acid 4-Tolylboronic acid 2-Borono-3-bromo-6-fluoroanisole 2-(Benzyloxy)-5-methoxyphenylboronicacid 3-Bromo-2-chloro-6-methoxyphenylboronic acid 2-BENZYLOXY-5-FORMYL-3-METHOXYPHENYLBORONIC ACID 3,5-DICHLORO-4-METHOXYPHENYLBORONIC ACID Ethyl 2-(Chlorosulfonyl)acetate 2-BROMO-5-METHOXYPHENYLBORONIC ACID 3,4,5-Trimethoxyphenylboronic acid Ascoric Acid 5-Methyl-2-methoxyphenylboronic acid 2-Ethoxy-5-methoxybenzeneboronic acid m-Anisyl alcohol 2,6-DIFLUORO-4-METHOXYPHENYLBORONIC ACID 3-Bromo-6-fluoro-2-methoxyphenylboronic acid 3-Bromo-2-fluoro-6-methoxyphenylboronicacid 3-CHLORO-2-METHOXYPHENYLBORONIC ACID
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