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Merck
CN

465232

4-Bromo-2-fluorobenzaldehyde

96%

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About This Item

Linear Formula:
BrC6H3(F)CHO
CAS Number:
Molecular Weight:
203.01
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Assay:
96%
Form:
solid
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assay

96%

form

solid

mp

58-62 °C (lit.)

functional group

aldehyde, bromo, fluoro

SMILES string

Fc1cc(Br)ccc1C=O

InChI

1S/C7H4BrFO/c8-6-2-1-5(4-10)7(9)3-6/h1-4H

InChI key

UPCARQPLANFGQJ-UHFFFAOYSA-N

Application

4-Bromo-2-fluorobenzaldehyde has been used in the preparation of:
  • 2-functionalized aromatic monoaldehydes, via reaction with different secondary amines and phenol
  • fluorostilbenes
  • benzyl amine-based histamine H3 antagonist having serotonin reuptake activity
  • 6-bromo-2-(4-bromo-2-fluorophenyl)-2,3-dihydro-4H-chromen-4-one


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Michael A Letavic et al.
Bioorganic & medicinal chemistry letters, 17(17), 4799-4803 (2007-07-10)
The design, synthesis, and in vitro activity of a series of novel 5-ethynyl-2-aryloxybenzylamine-based histamine H(3) ligands that are also serotonin reuptake transporters is described.
Richard J Sciotti et al.
Bioorganic & medicinal chemistry letters, 12(16), 2121-2123 (2002-07-20)
A novel series of antimicrobials of the oxazolidinone class is disclosed. These compounds are characterized relative to previously described analogues by a 'halostilbene-derived' pharmacophore and demonstrate enhanced antimicrobial activity against key Gram-positive pathogens when compared to Linezolid.
Hany F Nour et al.
Organic & biomolecular chemistry, 9(9), 3258-3271 (2011-03-25)
2-Functionalised aromatic monoaldehydes were synthesised in good to excellent yields by reacting 4-bromo-2-fluorobenzaldehyde with different secondary amines and phenol. The Suzuki-coupling reaction of the newly functionalised aromatic monoaldehydes with 4-formylphenylboronic acid afforded the corresponding 2-functionalised-4,4'-biphenyldialdehydes in good yields (47-85%). The



Global Trade Item Number

SKUGTIN
465232-25G04061831829952
465232-5G04061831811032