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2-Carboxyphenylboronic acid

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Company Name: Henan Fengda Chemical Co., Ltd
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Products Intro: Product Name:2-Carboxyphenylboronic acid
CAS:149105-19-1
Purity:99% Package:1kg;34USD|1000kg;1.2USD
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Products Intro: Product Name:2-carboxyphenylboronic acid
CAS:149105-19-1
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CAS:149105-19-1
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CAS:149105-19-1
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2-Carboxyphenylboronic acid manufacturers

  • 2-Carboxyphenylboronic acid
  • 2-Carboxyphenylboronic acid pictures
  • $34.00 / 1kg
  • 2025-09-25
  • CAS:149105-19-1
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
  • 2-Carboxyphenylboronic acid
  • 2-Carboxyphenylboronic acid pictures
  • $15.00 / 1KG
  • 2021-07-13
  • CAS:149105-19-1
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • Supply Ability: Monthly supply of 1 ton
  • 2-Carboxyphenylboronic acid
  • 2-Carboxyphenylboronic acid pictures
  • $15.00 / 1KG
  • 2021-07-10
  • CAS:149105-19-1
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • Supply Ability: Monthly supply of 1 ton
2-Carboxyphenylboronic acid Basic information
Product Name:2-Carboxyphenylboronic acid
Synonyms:2-BORONOBENZOIC ACID;2-CARBOXYBENZENEBORONIC ACID;2-CARBOXYPHENYLBORONIC ACID;(2-DIHYDROXYBORONYL)BENZOIC ACID;2-(DIHYDROXYBORYL)BENZOIC ACID;RARECHEM AH PB 0146;O-CARBOXYPHENYLBORONIC ACID;2-CarboxyphenylboronicAcid97+%
CAS:149105-19-1
MF:C7H7BO4
MW:165.94
EINECS:640-144-7
Product Categories:Pyrazines;Heterocyclic Compounds;Boronate Ester;Potassium Trifluoroborate;Substituted Boronic Acids;Boronic Acids & Esters;Phenyls & Phenyl-Het;Boronic acids;Aryl;Organoborons;Boronic acid;Boronic Acids & Esters;Phenyls & Phenyl-Het;blocks;BoronicAcids;Carboxes
Mol File:149105-19-1.mol
2-Carboxyphenylboronic acid Structure
2-Carboxyphenylboronic acid Chemical Properties
Melting point 138-141°C
Boiling point 412.3±47.0 °C(Predicted)
density 1.40±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,2-8°C
solubility soluble in Methanol
form powder to crystal
pka4.27±0.36(Predicted)
color White to Almost white
BRN 2835407
InChI1S/C7H7BO4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4,11-12H,(H,9,10)
InChIKeyKWNPRVWFJOSGMZ-UHFFFAOYSA-N
SMILESOB(O)c1ccccc1C(O)=O
CAS DataBase Reference149105-19-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-20/21/22-36/37
Safety Statements 26-36/37/39-36
WGK Germany WGK 3
Hazard Note Irritant/Keep Cold
HazardClass IRRITANT
HS Code 29319090
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
ALFA English
2-Carboxyphenylboronic acid Usage And Synthesis
Chemical PropertiesWhite powder
Uses2-Carboxyphenylboronic acid is used in the studies on a new class of carbohydrate-binding boronic acids called the boronophthalide; a sugar-binding boronic acids that is soluble and capable of complexing glycosides in neutral water.
Synthesis
Carbon dioxide

124-38-9

Boroxin, 2,4,6-tris(2-bromophenyl)-

1229227-01-3

2-Carboxyphenylboronic acid

149105-19-1

The o-bromophenylboronic acid trimer was dissolved in 600 mL of anhydrous tetrahydrofuran under nitrogen protection. After homogenization, the solution was transferred to a 2 L three-neck flask and cooled to -10 °C. Under the condition of maintaining temperature, 1.2 L of 1 M isopropylmagnesium chloride solution (1.2 moles) was added slowly and dropwise. After the dropwise addition, the reaction was continued to be stirred at -10 °C for 1-3 hours. Subsequently, the reaction system was allowed to warm up naturally to room temperature and stirring was continued for 2-5 hours. The reaction system was cooled to 0 °C again, dry ice was added in three batches, the reaction was stirred and the reaction progress was monitored by TLC. Upon completion of the reaction, the reaction was quenched with 15% aqueous hydrochloric acid, the pH was adjusted to 1-2, and stirring was continued for 3-5 hours at room temperature to ensure complete hydrolysis of the trimer. After precipitation of the solid, it was filtered and recrystallized from a mixed solvent of water and ethanol to give 81.4 g of white solid o-carboxyphenylboronic acid with HPLC purity of 98.4%. The overall yield of the two-step reaction was 49%.

References[1] Patent: CN104844643, 2017, B. Location in patent: Paragraph 0032; 0033
2-Carboxyphenylboronic acid Preparation Products And Raw materials
Raw materialsCarbon dioxide-->Boroxin, 2,4,6-tris(2-bromophenyl)--->ISOPROPYLMAGNESIUM CHLORIDE-->Tetrahydrofuran
Preparation ProductsOTAVA-BB 1364602
Tag:2-Carboxyphenylboronic acid(149105-19-1) Related Product Information
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