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Home > Encyclopedia > B-(2-Aminophenyl)boronic acid

B-(2-Aminophenyl)boronic acid

B-(2-Aminophenyl)boronic acid structure

B-(2-Aminophenyl)boronic acid 

structure
  • CAS No:

    5570-18-3

  • Formula:

    C6H8BNO2

  • Chemical Name:

    B-(2-Aminophenyl)boronic acid

  • Synonyms:

    Boronic acid,B-(2-aminophenyl)-;Benzeneboronic acid,o-amino-;Boronic acid,(2-aminophenyl)-;B-(2-Aminophenyl)boronic acid;2-Aminobenzeneboronic acid;2-Aminophenylboronic acid;o-Aminophenylboronic acid

Description

Crystalline powder

B-(2-Aminophenyl)boronic acid Basic Attributes

136.94

136.94

2962939

29310095

Characteristics

66.5

-0.47020

1.2±0.1 g/cm3

175-176 °C

346.9°C at 760 mmHg

163.6±28.4 °C

1.582

Safety Information

36/37/38-20/21/22

26-36/37/39-37-36

Xi,Xn

Harmful

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 7 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

B-(2-Aminophenyl)boronic acid Use and Manufacturing

The reaction flask was charged with compound II (8 g, 47.9 mmol), ethanol (40 ml) and water (60 ml) under a 50 ° C oil bath. Under nitrogen protection, iron powder (16 g) and concentrated hydrochloric acid (0.5 ml) were added and incubated for 3 hr. After completion of the reaction, ethanol (80 ml) was added to the reaction mixture, and the mixture was filtered through celite to obtain a light brown syrup. Concentrated under reduced pressure as a brown solid, recrystallized from 50percent ethanol, filtered and dried to give a pale gray color compound (5.5 g) in 83percent yield.A mixture of 84A (1.0 g, 6 mmol) and 10percent Pd/C (50 mg) in EtOH (50 mL) was hydrogenated in a Paar shaker at 1 bar for 8 hours. The mixture was filtered through a pad of celite and the filtrate was concentrated. The resulting residue was triturated with hexanes and the resulting solid was filtered to afford 84B (0.4g, 50percent).(i)(i) The 1.10g to iodine aniline (5mmol), 1.40g connecting boric acid pinacone ester (5.5mmol), 1.45g acetic acid potassium (15mmol) and PdCl

Computed Properties

Molecular Weight:136.95
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:137.0648087
Monoisotopic Mass:137.0648087
Topological Polar Surface Area:66.5
Heavy Atom Count:10
Complexity:110
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Material

Nitric acid

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