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4-Brom-2-fluorbenzaldehyd
96%
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About This Item
Lineare Formel:
BrC6H3(F)CHO
CAS-Nummer:
Molekulargewicht:
203.01
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
Empfohlene Produkte
Assay
96%
Form
solid
mp (Schmelzpunkt)
58-62 °C (lit.)
Funktionelle Gruppe
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
InChIKey
UPCARQPLANFGQJ-UHFFFAOYSA-N
Anwendung
4-Bromo-2-fluorobenzaldehyde has been used in the preparation of:
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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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
Simona Rapposelli et al.
Archiv der Pharmazie, 344(6), 372-385 (2011-02-15)
Aldose reductase (ARL2) is the first enzyme in the polyol pathway which catalyzes the NADPH-dependent reduction of glucose to sorbitol. Its involvement on diabetic complications makes this enzyme a challenge therapeutic target widely investigated to limit and/or prevent them. On
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