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521027 Aldrich

trans-1-Octen-1-ylboronic acid

Synonym: (2E)-2-Octen-1-ylboronic acid, (E)-1-Octen-1-ylboronic acid, (E)-1-Octenylboronic acid, trans-1-Octenylboronic acid

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Properties

Related Categories Alkenyl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents More...
InChI Key   RBTAJLKAPFBZDQ-BQYQJAHWSA-N
mp   100-104 °C(lit.)

Description

Other Notes

Contains varying amounts of anhydride

Packaging

1 g in glass bottle

Application

Reactant for:
• Chiral palladacycle-catalyzed asymmetric ring-opening reaction
• Enantioselective conjugate addition catalyzed by acyltartaric acids
• Copper-mediated oxidative cross-coupling reactions
• Diastereoselective domino Heck-Suzuki reactions

Price and Availability


KitAlysis - Increasing Catalysis Productivity

Cross-Coupling Guide
Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Boronic Acids - Aldrich ChemFiles 2007, 7.7, 3.

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...
Aldrich ChemFiles 2007, 7.7, 3.
Keywords: Chemfiles, Coupling reactions, Dehydration reaction, Suzuki coupling

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