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A71751 Sigma-Aldrich

3-Aminophenylboronic acid hemisulfate salt

≥95%

Synonym: (3-aminophenyl)-boronic acid sulfate (2:1), (3-Aminophenyl)boric acid hemisulfate, (m-Aminophenyl)boronic acid hemisulfate, 3-Aminobenzeneboronic acid hemisulfate salt, Bis[3-dihydroxyboranyl)benzenaminium] sulfate

  • CAS Number 66472-86-4

  • Linear Formula H2NC6H4B(OH)2 · 0.5H2SO4

  • Molecular Weight 185.98

  •  Beilstein/REAXYS Number 8094151

  •  EC Number 266-376-5

  •  MDL number MFCD00013111

  •  PubChem Substance ID 24891184

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids,
InChI Key   UKTAURVTSWDIQR-UHFFFAOYSA-N
assay   ≥95%
mp   ≥300 °C

Description

Packaging

25 g in poly bottle

5 g in glass bottle

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 (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

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