Search
Element Search
Structure Search
Thermo Scientific Chemicals
3-Bromo-4-hydroxybenzaldehyde, 97+%
CAS: 2973-78-6 | C7H5BrO2 | 201.02 g/mol
Have Questions?
Change view
Catalog number B24729.06
also known as B24729-06
Price (USD)
39.65
Special offer
Online exclusive
Ends: 30-Jun-2026
46.50Save 6.85 (15%)
Each
Quantity:
5 g
Price (USD)
39.65
Special offer
Online exclusive
Ends: 30-Jun-2026
46.50Save 6.85 (15%)
Each
Chemical Identifiers
CAS2973-78-6
Specifications
Specification Sheet
Specification SheetAppearance (Color)White to cream to pale brown
Assay (GC)≥97.0%
FormPowder
Identification (FTIR)Conforms
Melting Point (clear melt)122.0-131.0°C
3-Bromo-4-hydroxybenzaldehyde is an intermediate in organic syntheses, it is used to produce other chemicals like 5-Brom-4-hydroxy-b-nitrostyrol.
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
3-Bromo-4-hydroxybenzaldehyde is an intermediate in organic syntheses, it is used to produce other chemicals like 5-Brom-4-hydroxy-b-nitrostyrol.
Solubility
Soluble in water 1.33 g/L.
Notes
Air sensitive. Store under dry inert gas. Store away from oxidizing agents, air.
3-Bromo-4-hydroxybenzaldehyde is an intermediate in organic syntheses, it is used to produce other chemicals like 5-Brom-4-hydroxy-b-nitrostyrol.
Solubility
Soluble in water 1.33 g/L.
Notes
Air sensitive. Store under dry inert gas. Store away from oxidizing agents, air.
RUO – Research Use Only
General References:
- S.L. Manley; D.J. Chapman. Formation of 3-bromo-4-hydroxybenzaldehyde from L-tyrosine in cell-free homogenates of Odonthalia floccosa (Rhodophyceae): a proposed biosynthetic pathway for brominated phenols. FEBS LETTERS. 1978, 93 (1), 97-101.
- Steven L. Manley; David J. Chapman. Metabolism of 4-hydroxybenzaldehyde, 3-bromo-4-hydroxybenzaldehyde and bromide by cell-free fractions of the marine red alga Odonthalia floccosa. Phytochemistry. 1980, 19 (7), 1453-1457.