Search Thermo Fisher Scientific
Element Search
Structure Search
Thermo Scientific Chemicals
3,4-Dibromobenzaldehyde, 99%
CAS: 74003-55-7 | C7H4Br2O | 263.916 g/mol
Have Questions?
Change view
Catalog number ALFL13762.06
View Price:Sign InSign in to see your account pricing. Need an account? Register with us today.
Quantity:
5 g
Specifications
Chemical Name or Material3,4-Dibromobenzaldehyde
CAS74003-55-7
Health Hazard 1H315-H319-H335
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
View more
3,4-Dibromobenzaldehyde is used in the preparation of isomeric branched pi-conjugated system with terminal alkyne by reacting with 4-(triisopropylsilylethynyl) phenylacetylene.
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
3,4-Dibromobenzaldehyde is used in the preparation of isomeric branched pi-conjugated system with terminal alkyne by reacting with 4-(triisopropylsilylethynyl) phenylacetylene.
Solubility
Insoluble in water.
Notes
Air sensitive. Incompatible with strong oxidizing agents.
3,4-Dibromobenzaldehyde is used in the preparation of isomeric branched pi-conjugated system with terminal alkyne by reacting with 4-(triisopropylsilylethynyl) phenylacetylene.
Solubility
Insoluble in water.
Notes
Air sensitive. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Onal, E.; Yerli, Y.; Cosut, B.; Pilet, G.; Ahsen, V.; Luneau, D.; Hirel, C. Nitronyl and imino nitroxide free radicals as precursors of magnetic phthalocyanine and porphyrin building blocks. New J. Chem. 2014, 38 (9), 4440-4447.
- Biet, T.; Fihey, A.; Cauchy, T.; Vanthuyne, N.; Roussel, C.; Crassous, J.; Avarvari, N. Ethylenedithio-Tetrathiafulvalene-Helicenes: Electroactive Helical Precursors with Switchable Chiroptical Properties. Chem. Eur. J. 2013, 19 (39), 13160-13167.