3-Methoxy-4-methylbenzeneboronic acid, 97%

3-Methoxy-4-methylbenzeneboronic acid, 97% Suppliers list
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Products Intro: Product Name:3-methoxy-4-methylphenylboronic acid
CAS:917757-15-4
Purity:97% (Min,HPLC) Package:1G;1KG;100KG
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Products Intro: Product Name:3-Methoxy-4-methylphenylboronic acid
CAS:917757-15-4
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Products Intro: Product Name:3-Methoxy-4-methylphenylboronic acid
CAS:917757-15-4
Purity:0.98 Package:1g;5g;25g;5222g
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Products Intro: Product Name:3-METHOXY-4-METHYLPHENYLBORONIC ACID
CAS:917757-15-4
Purity:99% Package:1kg

3-Methoxy-4-methylbenzeneboronic acid, 97% manufacturers

3-Methoxy-4-methylbenzeneboronic acid, 97% Basic information
Product Name:3-Methoxy-4-methylbenzeneboronic acid, 97%
Synonyms:3-Methoxy-4-methylbenzeneboronic acid, 97%;Boronic acid, B-(3-methoxy-4-methylphenyl)-;B-(3-Methoxy-4-methylphenyl)boronic acid;3-Methoxy-4-methylbenzeneboronic acid, 97%
CAS:917757-15-4
MF:C8H11BO3
MW:165.98
EINECS:
Product Categories:Boronate Ester;Boronic Acid;Potassium Trifluoroborate
Mol File:917757-15-4.mol
3-Methoxy-4-methylbenzeneboronic acid, 97% Structure
3-Methoxy-4-methylbenzeneboronic acid, 97% Chemical Properties
Melting point 192-194°C
Boiling point 318.3±52.0 °C(Predicted)
density 1.14±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka8.36±0.10(Predicted)
AppearanceWhite to off-white Solid
Water Solubility Slightly soluble in water.
Safety Information
HS Code 2931900090
MSDS Information
3-Methoxy-4-methylbenzeneboronic acid, 97% Usage And Synthesis
UsesIt is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.
Synthesis
Triisopropyl borate

5419-55-6

4-BROMO-2-METHOXYTOLUENE

67868-73-9

3-Methoxy-4-methylbenzeneboronic acid, 97%

917757-15-4

Butyl lithium (1.6 M in hexane, 3.75 mL) was slowly added dropwise to a stirred solution of 2-methyl-5-bromoanisole (5 mmol) in tetrahydrofuran (20 mL) at -78 °C for 45 min. Subsequently, triisopropyl borate (1.75 mL, 7.5 mmol) was added to the reaction system. The reaction mixture was allowed to slowly warm to -30°C, and then 2.5 N hydrochloric acid (10 mL) was added. The mixture was gradually warmed to room temperature with stirring and diluted with ethyl acetate. The organic and aqueous layers were separated and the aqueous layer was extracted twice with ethyl acetate. The organic layers were combined, washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuum. Purification of the crude product using fast column chromatography (elution gradient: 0-40% ethyl acetate/hexane) gave 3-methoxy-4-methylphenylboronic acid as a white powder.

References[1] European Journal of Medicinal Chemistry, 2018, vol. 149, p. 79 - 89
3-Methoxy-4-methylbenzeneboronic acid, 97% Preparation Products And Raw materials
Raw materials4-BROMO-2-METHOXYTOLUENE-->Triisopropyl borate-->Hydrochloric acid-->n-Butyllithium-->Tetrahydrofuran-->Hexane
Tag:3-Methoxy-4-methylbenzeneboronic acid, 97%(917757-15-4) Related Product Information
4-Tolylboronic acid 3-difluoromethoxy-4-methyl-benzeneboronic acid 3-METHOXY-4-METHOXYCARBONYLPHENYLBORONIC ACID, PINACOL ESTER 3 3-METHOXY-4-CARBOXYPHENYLBORONIC ACID 3-Acetoxy-4-methoxycarbonylphenylboronic acid, pinacol ester 3-Benzyloxy-4-methoxycarbonylphenylboronic acid, pinacol ester 2-(2,3-DIHYDROBENZOFURAN-6-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE 4-ETHOXYCARBONYL-3-METHOXYPHENYLBORONIC ACID 3-Methoxy-4-methylbenzeneboronic acid, 97% 2,4-DIMETHYL-3-METHOXYBENZENEBORONIC ACID (4-FORMYL-3-METHOXYPHENYL)BORONIC ACID Boronic acid, (4-cyano-3-methoxyphenyl)- (9CI) 5-CHLORO-4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)-2-METHOXYBENZOIC ACID

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