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675180 Aldrich

Isoquinoline-5-carboxaldehyde

96%

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Properties

Related Categories Aldehydes, Building Blocks, C10-C12, Carbonyl Compounds, Chemical Synthesis,
InChI Key   ILRSABOCKMOFGW-UHFFFAOYSA-N
assay   96%
mp   116-120 °C

Description

Application

Direct conversion of heteroaryl-carboxaldehydes to acetonitriles by treatment with cyanoethylphosphonate followed by samarium(II) iodide reduction.

Packaging

1 g in glass bottle

Price and Availability

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Aldehydes

Hartmann and co-workers have described the synthesis of a series of potent and selective inhibitors of aldosterone synthase (CYP11B2), in which the key synthetic step was a Wittig reaction using vari...
Aldrich ChemFiles 2007, 7.8, 3.
Keywords: Addition reactions, Aldol reaction, Asymmetric synthesis, Building blocks, Chemfiles, Wittig Reaction

Peer-Reviewed Papers
15

References

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