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596256 Sigma-Aldrich

trans-(2-Cyclohexylvinyl)boronic acid

95%

Synonym: (E)-(2-Cyclohexylvinyl)boronic acid, trans-(2-Cyclohexylethenyl)boronic acid

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Properties

Related Categories Alkenyl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents More...
Quality Level   100
assay   95%
mp   106-111 °C (lit.)
storage temp.   2-8°C
SMILES string   OB(O)\C=C\C1CCCCC1
InChI   1S/C8H15BO2/c10-9(11)7-6-8-4-2-1-3-5-8/h6-8,10-11H,1-5H2/b7-6+
InChI key   FBRJOMMIILHLCG-VOTSOKGWSA-N

Description

Application

Reactant for:
• Pd-catalyzed coupling reactions
• Chiral palladacycle-catalyzed asymmetric ring-opening reaction
• Asymmetric Suzuki-Miyaura coupling

Packaging

1, 10 g in glass bottle

Other Notes

Contains varying amounts of anhydride

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3
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

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