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4-(Trifluoromethyl)benzaldehyde, 97%
CAS: 455-19-6 | C8H5F3O | 174.122 g/mol
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Catalog number ALFA15276.14
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Quantity:
25 g
Specifications
Chemical Name or Material4-(Trifluoromethyl)benzaldehyde
CAS455-19-6
Health Hazard 1H227-H315-H319-H320-H335
Health Hazard 2GHS H Statement
H302-H315-H319-H335-H227
Harmful if swallowed.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Combustible liquid.
H302-H315-H319-H335-H227
Harmful if swallowed.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Combustible liquid.
Health Hazard 3P210-P235-P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P370+P378q-P501c
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4-(Trifluoromethyl)benzaldehyde is useful reagent in kinetic studies of the asymmetric synthesis of alcohols and of the Wittig reaction. It is also used as Pharmaceutical intermediates.
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
4-(Trifluoromethyl)benzaldehyde is useful reagent in kinetic studies of the asymmetric synthesis of alcohols and of the Wittig reaction. It is also used as Pharmaceutical intermediates.
Solubility
Soluble in water. 1.5 g/L at 20°C
Notes
Air Sensitive. Store away from air and oxidizing agents. Store under an inert atmosphere. Incompatible with oxidizing agents, reducing agents.
4-(Trifluoromethyl)benzaldehyde is useful reagent in kinetic studies of the asymmetric synthesis of alcohols and of the Wittig reaction. It is also used as Pharmaceutical intermediates.
Solubility
Soluble in water. 1.5 g/L at 20°C
Notes
Air Sensitive. Store away from air and oxidizing agents. Store under an inert atmosphere. Incompatible with oxidizing agents, reducing agents.
RUO – Research Use Only
General References:
- Raymond J. Abraham; Simone Angioloni; Mark Edgar and Fernando Sancassan. Conformational analysis. Part 29.1 The conformationalanalysis of 2-substituted fluoro- and trifluoromethyl-benzaldehydes,acetophenones and methyl benzoates by the lanthanide induced shift(LIS)technique.J. Chem. Soc., Perkin Trans. 2.1997, 41-48.
- D C Anderson and F W Dahlquist. Determination of the equilibrium distribution between alcohol and aldehyde substrates when bound to horse liver alcohol dehydrogenase using magnetic resonance.Biochemistry (Washington).1980, 19, (24), 5486-5493 .