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521396 Sigma-Aldrich

2-Cyanophenylboronic acid

≥95.0%

Synonym: 2-Cyanobenzeneboronic acid, [m-Cyanophenyl-4-yl]boronic acid

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids,
InChI Key   NPLZNDDFVCGRAG-UHFFFAOYSA-N
assay   ≥95.0%
mp   240 °C (dec.) (lit.)

Description

Packaging

1, 5 g in glass bottle

Application

Employed in a rhodium-catalyzed [3+2] annulation with alkynes leading to substituted indenones.

Useful in the synthesis of substitutes indenones or indanones

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

Documents

Certificate of Analysis

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Certificate of Origin

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Protocols & Articles

Articles

Boronic Acids - ChemFiles 2007

Most boronic acids readily undergo dehydration reactions to give a cyclic (trimer) anhydride. Our selection of boronic acids may contain varying amounts of this cyclic anhydride. Fortunately, the aci...
ChemFiles 2007, 7.7, 3.
Keywords: Coupling reactions, Dehydration reaction, Suzuki coupling

Peer-Reviewed Papers
15

References

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