Nucleic Acid Synthesis

Application Employed in a rhodium-catalyzed [3+2] annulation with alkynes leading to substituted indenones. Useful in the synthesis of substitutes indenones or indanones

May contain varying amounts of anhydride. Application Reactant involved in: Reactions with (cyanomethylphenyl)boronic acid Synthesis of oligo-boronic acid receptors with improved structural and electronic properties Syntesis of

May contain varying amounts of anhydride. Application Reactant involved in: Reactions with (cyanomethylphenyl)boronic acid Synthesis of oligo-boronic acid receptors with improved structural and electronic properties Syntesis of

Analysis Note Assay (GC, area%): &#8805 96.0 % (a/a) Melting range (lower value): &#8805 74 &#176C Melting range (upper value): &#8804 77 &#176C Identity (IR): passes test

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 0.

Analysis Note Assay isomers (GC, area%): &#8805 99.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 0.

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Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

for synthesis Analysis Note Assay (HClO&#8324): &#8805 98.0 % Identity (IR): passes test

Application 4-Cyanophenylboronic acid can be used as a reactant in: Palladium-catalyzed Suzuki-Miyaura cross-coupling in water. Ruthenium catalyzed direct arylation of benzylic sp 3 carbons of acyclic amines with arylboronates.

Application 4-Cyanophenylboronic acid can be used as a reactant in: Palladium-catalyzed Suzuki-Miyaura cross-coupling in water. Ruthenium catalyzed direct arylation of benzylic sp 3 carbons of acyclic amines with arylboronates.

Analysis Note Assay (GC, area%): &#8805 96.5 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 0.