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Thermo Scientific Chemicals
2-Bromobenzaldehyde, 98%
CAS: 6630-33-7 | C7H5BrO | 185.02 g/mol
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Catalog number A15065.36
also known as A15065-36
Price (EUR)
528,00
Each
Quantity:
500 g
Price (EUR)
528,00
Each
Chemical Identifiers
CAS6630-33-7
Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to pale yellow
FormLiquid
Assay (GC)≥97.5%
Free acid (titration)≤2.0%
Refractive Index1.5940-1.5980 @ 20?C
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2-Bromobenzaldehyde is used in L-threonine aldolase-catalyzed enantio and diastereoselective aldol reactions. Further, it reacts with trichloromethane to prepare 1-(2-bromo-phenyl)-2,2,2-trichloro-ethanol.
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-Bromobenzaldehyde is used in L-threonine aldolase-catalyzed enantio and diastereoselective aldol reactions. Further, it reacts with trichloromethane to prepare 1-(2-bromo-phenyl)-2,2,2-trichloro-ethanol.
Solubility
Soluble in alcohol and benzene. Insoluble in water.
Notes
Air sensitive. Incompatible with strong bases, strong oxidizing agents and strong reducing agents.
2-Bromobenzaldehyde is used in L-threonine aldolase-catalyzed enantio and diastereoselective aldol reactions. Further, it reacts with trichloromethane to prepare 1-(2-bromo-phenyl)-2,2,2-trichloro-ethanol.
Solubility
Soluble in alcohol and benzene. Insoluble in water.
Notes
Air sensitive. Incompatible with strong bases, strong oxidizing agents and strong reducing agents.
RUO – Research Use Only
General References:
- Vinoth, P.; Vivekanand, T.; Suryavanshi, P. A.; Menéndez, J. C.; Sasai, H.; Sridharan, V. Palladium(II)-catalyzed intramolecular carboxypalladation-olefin insertion cascade: direct access to indeno[1,2-b]furan-2-ones. Org. Biomol. Chem. 2015, 13 (18), 5175-5181.
- Saoudi, B.; Teniou, A.; Debache, A.; Roisnel, T.; Soulé, J. F.; Doucet, H. Cyclisation reaction between 3-methylquinoxaline-2-thione and benzaldehydes into 3-benzyl-2-aryl-thieno[2,3-b]quinoxaline promoted by Brønsted acids. C.R. Chim. 2015, 18 (8), 808-815.