ChemicalBook--->CAS DataBase List--->59142-68-6

59142-68-6

59142-68-6 Structure

59142-68-6 Structure
IdentificationMore
[Name]

2-Bromo-4-fluorobenzaldehyde
[CAS]

59142-68-6
[Synonyms]

2-BROMO-4-FLUOROBENZALDEHYDE
[Molecular Formula]

C7H4BrFO
[MDL Number]

MFCD00672923
[Molecular Weight]

203.01
[MOL File]

59142-68-6.mol
Chemical PropertiesBack Directory
[Melting point ]

61.5
[Boiling point ]

234.9±20.0 °C(Predicted)
[density ]

1.70
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

powder to crystal
[color ]

White to Light yellow
[InChI]

InChI=1S/C7H4BrFO/c8-7-3-6(9)2-1-5(7)4-10/h1-4H
[InChIKey]

OPZDXMCOWFPQPE-UHFFFAOYSA-N
[SMILES]

C(=O)C1=CC=C(F)C=C1Br
[CAS DataBase Reference]

59142-68-6(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
[Hazard Codes ]

Xi
[Risk Statements ]

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 .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT, LIGHT SENSITIVE
[HS Code ]

29122990
Hazard InformationBack Directory
[Chemical Properties]

White to light yellow solid
[Uses]

2-Bromo-4-fluorobenzaldehyde used as pharmaceutical intermediates.It could be the starting material to synthesise 2-Bromo-4-fluorobenzonitrile, 6-Fluoroisobenzofuran-1(3H)-one, etc.
[Synthesis]

2-BROMO-4-FLUOROBENZYL ALCOHOL

229027-89-8

2-Bromo-4-fluorobenzaldehyde

59142-68-6

The general procedure for the synthesis of 2-bromo-4-fluorobenzaldehyde from 2-bromo-4-fluorobenzyl alcohol was as follows: benzyl alcohol substrate (0.2 mmol), FeCl3-6H2O (0.002 mmol, 5.4 mg) and triphenylmethanol (0.2 mmol, 52 mg) were mixed in a dry reaction vessel. Subsequently, the reaction mixture was irradiated in a microwave reactor at 55 °C for 1 hour. Upon completion of the reaction, the crude product was purified by fast column chromatography to afford the target product 2-bromo-4-fluorobenzaldehyde.

[References]

[1] Tetrahedron, 2015, vol. 71, # 38, p. 6744 - 6748
[2] Synthesis (Germany), 2013, vol. 45, # 24, p. 3387 - 3391
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