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BENZOFURAN-5-BORONIC ACID

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Company Name: Alchem Pharmtech,Inc.
Tel: 8485655694
Email: sales@alchempharmtech.com
Products Intro: Product Name:Benzofuran-5-ylboronic acid
CAS:331834-13-0
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-59125
Company Name: Nanjing jinheyou Trading Co., Ltd.
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Products Intro: Product Name:BENZOFURAN-5-BORONIC ACID
CAS:331834-13-0
Purity:95%min Package:1g;USD
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Products Intro: Product Name:BENZOFURAN-5-BORONIC ACID
CAS:331834-13-0
Purity:99% Package:1kg
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Products Intro: Product Name:BENZOFURAN-5-BORONIC ACID
CAS:331834-13-0
Purity:99% Package:1KG;1USD
Company Name: Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
Tel: +8613580539051
Email: joe@yuhengpharm.com
Products Intro: Product Name:benzofuran-5-ylboronic acid
CAS:331834-13-0
Purity:0.97 Package:1KG;25KG

BENZOFURAN-5-BORONIC ACID manufacturers

BENZOFURAN-5-BORONIC ACID Basic information
Product Name:BENZOFURAN-5-BORONIC ACID
Synonyms:5-Benzofuranylboronic acid;Boronic acid, B-5-benzofuranyl-;1-Benzofuran-5-boronic acid, 5-Borono-1-benzofuran;ENZOFURAN-5-BORONIC ACID;BENZOFURAN-5-BORONIC ACID;AKOS BRN-0183;Akos ba-183;benzofuran-5-yl-5-boronic acid
CAS:331834-13-0
MF:C8H7BO3
MW:161.95
EINECS:
Product Categories:
Mol File:331834-13-0.mol
BENZOFURAN-5-BORONIC ACID Structure
BENZOFURAN-5-BORONIC ACID Chemical Properties
Boiling point 340.4±34.0 °C(Predicted)
density 1.31±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,2-8°C
form solid
pka8.25±0.30(Predicted)
color White to off-white
InChIInChI=1S/C8H7BO3/c10-9(11)7-1-2-8-6(5-7)3-4-12-8/h1-5,10-11H
InChIKeyWYXQQAYIAJRORT-UHFFFAOYSA-N
SMILESB(C1=CC=C2OC=CC2=C1)(O)O
CAS DataBase Reference331834-13-0(CAS DataBase Reference)
Safety Information
Hazard Codes C
Hazard Note Corrosive
HS Code 2932990090
MSDS Information
BENZOFURAN-5-BORONIC ACID Usage And Synthesis
Synthesis
5-Bromo-1-benzofuran

23145-07-5

Trimethyl borate

121-43-7

BENZOFURAN-5-BORONIC ACID

331834-13-0

The general procedure for the synthesis of benzo[b]furan-5-boronic acid from 5-bromobenzo[b]furan and trimethyl borate is as follows: 1. a hexane solution of n-butyllithium (1.5 M; 3.72 ml, 5.6 mmol) was slowly added dropwise to a solution of tetrahydrofuran (10 ml) of 5-bromobenzo[b]furan (1.0 g, 5.0 mmol) under argon protection, keeping the reaction temperature at -60°C. 2. stirring was continued at the same temperature for 30 min. 3. trimethyl borate (0.69 ml, 6.0 mmol) was added to the reaction system, followed by slow warming of the reaction mixture to room temperature over a period of 4 hours. 4. Water (5 ml) was added to the reaction mixture and cooled to 5 °C, followed by distillation under reduced pressure to remove the tetrahydrofuran. 5. The pH was adjusted to 1 by adding 1N hydrochloric acid to the residue and then extracted with ethyl acetate. 6. The organic layer was washed with brine, dried and the solvent was removed by distillation. 7. The residue was ground with hexane/ether mixture, filtered and dried to give benzo[b]furan-5-boronic acid (551 mg) in light brown solid form.

References[1] Patent: EP2959918, 2015, A1. Location in patent: Paragraph 0089
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