ChemicalBook--->CAS DataBase List--->248274-03-5

248274-03-5

248274-03-5 Structure

248274-03-5 Structure
IdentificationBack Directory
[Name]

2-(AMINOMETHYL)PHENYL BORONIC ACID
[CAS]

248274-03-5
[Synonyms]

2-(AMINOMETHYL)PHENYL BORONIC ACID
2-(Aminomethyl)phenyl boronic acid 95%
Boronic acid, B-[2-(aminomethyl)phenyl]-
[Molecular Formula]

C7H10BNO2
[MDL Number]

MFCD06212997
[MOL File]

248274-03-5.mol
[Molecular Weight]

150.97
Chemical PropertiesBack Directory
[Boiling point ]

354.0±44.0 °C(Predicted)
[density ]

1.18±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

8.23±0.53(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2931900090
Spectrum DetailBack Directory
[Spectrum Detail]

2-(AMINOMETHYL)PHENYL BORONIC ACID(248274-03-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Cyanophenylboronic acid

138642-62-3

2-(AMINOMETHYL)PHENYL BORONIC ACID

248274-03-5

The general procedure for the synthesis of (2-(aminomethyl)phenyl)boronic acid from 2-cyanophenylboronic acid was as follows: to a methanol solution (20 mL) containing 2-cyanophenylboronic acid (300 mg, 2.0 mmol) was added nickel ryenne (100 mg, 10% w/w). The reaction mixture was stirred for 4 h at room temperature under hydrogen pressure of 50 psi. Upon completion of the reaction, the reaction mixture was filtered through a diatomaceous earth pad and the filtrate was concentrated under vacuum to afford (2-(aminomethyl)phenyl)boronic acid 150 mg (48.7% yield) as a white solid. Mass spectrum (electrospray positive ion mode): m/z = 152.20, 153.40, 154.35, 155.65 [M + H]+. Analyzed by liquid chromatography-mass spectrometry: retention time tR = 0.76 min.

[References]

[1] Patent: WO2015/81280, 2015, A1. Location in patent: Paragraph 00497; 00498
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