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2-Bromo-5-fluorobenzaldehyde, 98%, Thermo Scientific Chemicals
Catalog number: B25071.06
5 g, Each
Thermo Scientific Chemicals
2-Bromo-5-fluorobenzaldehyde, 98%, Thermo Scientific Chemicals
Catalog number: B25071.06
5 g, Each
Quantity
Catalog number: B25071.06
also known as B25071-06
Price (USD)
72.40
Each
Quantity
-
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Chemical Identifiers
CAS
94569-84-3
IUPAC Name
2-bromo-5-fluorobenzaldehyde
Molecular Formula
C7H4BrFO
InChI Key
CJUCIKJLMFVWIS-UHFFFAOYSA-N
SMILES
FC1=CC=C(Br)C(C=O)=C1
Specifications
Specification SheetAppearance (Color)
White to cream
Form
Crystals or powder or crystalline powder or fused/lumpy solid
Assay (GC)
≥97.5%
Free acid (titration)
≤1.5%
Melting Point (clear melt)
51.5-57.5?C
Description
2-Bromo-5-fluorobenzaldehyde is used as a precursor for the synthesis of 5-fluoro-3-substituted benzoxaboroles, which is used in material science as molecular receptors, building block in crystal engineering, as steroid conjugates for molecular imprinting , dyes and biosensors of alpha hydroxyl carboxylic acids. It is also used in the synthesis of 5-arylindazolo[3,2-b]quinazolin-7(5H)-one by reacting with 2-amino-N'-arylbenzohydrazide in the presence of Copper(I) bromide by the Ullmann-type reaction.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2-Bromo-5-fluorobenzaldehyde is used as a precursor for the synthesis of 5-fluoro-3-substituted benzoxaboroles, which is used in material science as molecular receptors, building block in crystal engineering, as steroid conjugates for molecular imprinting , dyes and biosensors of alpha hydroxyl carboxylic acids. It is also used in the synthesis of 5-arylindazolo[3,2-b]quinazolin-7(5H)-one by reacting with 2-amino-N′-arylbenzohydrazide in the presence of Copper(I) bromide by the Ullmann-type reaction.
Solubility
Soluble in methanol.
Notes
Air sensitive. Keep container tightly closed in a cool, dry and well-ventilated place.
2-Bromo-5-fluorobenzaldehyde is used as a precursor for the synthesis of 5-fluoro-3-substituted benzoxaboroles, which is used in material science as molecular receptors, building block in crystal engineering, as steroid conjugates for molecular imprinting , dyes and biosensors of alpha hydroxyl carboxylic acids. It is also used in the synthesis of 5-arylindazolo[3,2-b]quinazolin-7(5H)-one by reacting with 2-amino-N′-arylbenzohydrazide in the presence of Copper(I) bromide by the Ullmann-type reaction.
Solubility
Soluble in methanol.
Notes
Air sensitive. Keep container tightly closed in a cool, dry and well-ventilated place.
RUO – Research Use Only
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