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3-Carboxy-5-nitrophenylboronic acid

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Products Intro: Product Name:3-Carboxy-5-nitrophenylboronic acid
CAS:101084-81-5
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Products Intro: Product Name:3-Carboxy-5-nitrophenylboronic acid
CAS:101084-81-5
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CAS:101084-81-5
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CAS:101084-81-5
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Products Intro: Product Name:3-Carboxy-5-nitrophenylboronic acid
CAS:101084-81-5
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3-Carboxy-5-nitrophenylboronic acid manufacturers

3-Carboxy-5-nitrophenylboronic acid Basic information
Product Name:3-Carboxy-5-nitrophenylboronic acid
Synonyms:3-BORONO-5-NITROBENZOIC ACID;3-CARBOXY-5-NITROBENZENEBORONIC ACID;3-CARBOXY-5-NITROPHENYLBORONIC ACID;5-CARBOXY-3-NITROPHENYLBORONIC ACID;AKOS BRN-0156;RARECHEM AH PB 0071;3-Carboxy-5-Nitrophenylboronic;3-CARBOXY-5-NITROBENZOIC ACID
CAS:101084-81-5
MF:C7H6BNO6
MW:210.94
EINECS:205-516-1
Product Categories:blocks;BoronicAcids;Carboxes;Aryl;Nitro;Organoborons;Boronic acid
Mol File:101084-81-5.mol
3-Carboxy-5-nitrophenylboronic acid Structure
3-Carboxy-5-nitrophenylboronic acid Chemical Properties
Melting point 229°C(lit.)
Boiling point 502.6±60.0 °C(Predicted)
density 1.62±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form powder to crystal
pka3.49±0.10(Predicted)
color White to Light yellow
CAS DataBase Reference101084-81-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36
WGK Germany 3
HazardClass IRRITANT
HS Code 29319090
MSDS Information
3-Carboxy-5-nitrophenylboronic acid Usage And Synthesis
Chemical PropertiesWhite solid
UsesReactant for:
  • Copper-catalyzed chlorination
  • Parallel solid-phase synthesis of azabicyclooctylidenemethylbenzamides as μ- and d-opioid agonists

Used for:
  • Immobilization of glucose oxidase and acetylcholinesterase on boronic acid-activated silica surfaces
Usessuzuki reaction
Synthesis
3-Carboxyphenylboronic acid

25487-66-5

3-Carboxy-5-nitrophenylboronic acid

101084-81-5

The general procedure for the synthesis of 3-carboxy-5-nitrophenylboronic acid from 3-carboxyphenylboronic acid is as follows: first, 7.5 g of 3-carboxyphenylboronic acid (45.2 mmol) was mixed with 25 ml of concentrated sulphuric acid, and 25 ml of fuming nitric acid was slowly added under rapid stirring conditions while cooling using an ice water bath. The reaction mixture was stirred for 15 min, then the ice water bath was removed and the reaction continued to be stirred for 15 min. Subsequently, the reaction solution was poured into ice water to produce a precipitate, which was filtered and then the precipitate was washed with ice water for 5 times, and finally 6.01 g of 3-nitro-5-carboxyphenylboronic acid as a white solid was obtained by aqueous recrystallization in 63.0% yield. Next, 1.50 g of 3-carboxy-5-nitrophenylboronic acid (7.1 mmol) was dissolved in 20 ml of methanol, and 2 g of 10% Pd/C catalyst was added in a 50 ml three-necked flask for a catalytic hydrogenolysis reaction for 6 hours. After completion of the reaction, the Pd/C catalyst was removed by filtration and the filtrate was evaporated to dryness to give 1.25 g of 3-amino-5-carboxyphenylboronic acid as a white powdery solid in 97.1% yield.

References[1] Patent: CN103497211, 2016, B. Location in patent: Paragraph 0190
[2] Organic Preparations and Procedures International, 1991, vol. 23, # 6, p. 729 - 734
[3] Journal of the American Chemical Society, 1959, vol. 81, p. 3017
[4] Arkiv foer Kemi, 1957, vol. 10, p. 497,503
3-Carboxy-5-nitrophenylboronic acid Preparation Products And Raw materials
Raw materials3-Carboxyphenylboronic acid
Tag:3-Carboxy-5-nitrophenylboronic acid(101084-81-5) Related Product Information
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