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
- P-METHOXYPHENYLBORONIC ACID
- p-methoxybenzeneboronic acid
- p-Anisylboronic acid
- TIMTEC-BB SBB004055
- 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
- blocks
- BoronicAcids
- Organoborons
- B (Classes of Boron Compounds)
- organic or inorganic borate
- Aromatics
- Intermediates
- Miscellaneous Reagents
- Boronic Acid series
- Aryl Boronic Acids
- Boronic Acids and Derivatives
- Chemical Synthesis
- Monosubstituted Aryl Boronic Acids
- Organometallic Reagents
- Boron Derivatives
- Boronate Ester
- Potassium Trifluoroborate
- Morpholines/Thiomorpholines ,Isoxazoles ,Indazoles
- Mol File:
- 5720-07-0.mol
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.
- pka
- 8.96±0.10(Predicted)
- form
- Crystalline Powder
- color
- White to light beige
- BRN
- 2936912
- CAS DataBase Reference
- 5720-07-0(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
- Language:English Provider:4-Methoxyphenylboronic acid
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
4-Methoxyphenylboronic acid Usage And Synthesis
Chemical Properties
white to light beige crystalline powder
Uses
4-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.
Uses
4-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
Uses
4-Methoxylphenylboronic Acid is a phenylboronic acid used to investigate boron function in plants.
Uses
suzuki reaction
4-Methoxyphenylboronic acid Preparation Products And Raw materials
Preparation Products
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4-Methoxyphenylboronic acid(5720-07-0)Related Product Information
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- p-Anisaldehyde
- o-Anisaldehyde
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- (3-Methoxyphenyl)acetonitrile
- (Trifluoromethoxy)benzene
- Citric acid
- 4-Tolylboronic acid
- Ethyl 2-(Chlorosulfonyl)acetate
- 3-Methoxybenzaldehyde
- 4-Methoxyphenylacetic acid
- 4-Aminophenylboronic acid
- Hyaluronic acid
- 4-Methoxy-1H-indole-2-carboxylic acid
- 4-Chloropyridine-2-carboxylic acid
- 4-(METHOXYCARBONYL)PHENYLBORONIC ACID