ChemicalBook--->CAS DataBase List--->101084-81-5

101084-81-5

101084-81-5 Structure

101084-81-5 Structure
IdentificationMore
[Name]

3-Carboxy-5-nitrophenylboronic acid
[CAS]

101084-81-5
[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
3-CARBOXY-5-NITROPHENYLBORONIC ACID 97%
5-Carboxy-3-nitrobenzeneboronic acid, 97%
5-Nitro-3-carboxyphenylboronic acid
[EINECS(EC#)]

205-516-1
[Molecular Formula]

C7H6BNO6
[MDL Number]

MFCD00757433
[Molecular Weight]

210.94
[MOL File]

101084-81-5.mol
Chemical PropertiesBack Directory
[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
[pka]

3.49±0.10(Predicted)
[color ]

White to Light yellow
[CAS DataBase Reference]

101084-81-5(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29319090
Hazard InformationBack Directory
[Chemical Properties]

White solid
[Uses]

Reactant 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
[Uses]

suzuki 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
Spectrum DetailBack Directory
[Spectrum Detail]

3-Carboxy-5-nitrophenylboronic acid(101084-81-5)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

3-Carboxy-5-nitrobenzeneboronic acid, 97%(101084-81-5)
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