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480053 Sigma-Aldrich

4-tert-Butylphenylboronic acid

≥95.0%

Synonym: (p-tert-Butylphenyl)boronic acid, 4-t-Butylbenzeneboronic acid, 4-t-Butylphenylboronic acid, 4-tert-Butylbenzeneboronic acid, p-tert-Butylbenzeneboronic acid, [4-(1,1-Dimethylethyl)phenyl]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   MNJYZNVROSZZQC-UHFFFAOYSA-N
assay   ≥95.0%
mp   191-196 °C (lit.)

Description

Packaging

5, 25 g in glass bottle

Application

Cross-coupling building block used in synthesis of tetracycline derivatives.

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis (COA)

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Certificate of Origin (COO)

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Protocols & Articles

Articles

Arylboronic Acids

We are pleased to present its complete selection of arylboronic acids, the building blocks of the Suzuki coupling experiment. Most arylboronic acids readily undergo dehydration reactions to give a cy...
ChemFiles 2001, 1.1, 5.
Keywords: Building blocks, Coupling reactions, Dehydration reaction, Suzuki coupling

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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