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556599 Sigma-Aldrich

trans-2-Chloromethylvinylboronic acid

≥95%

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Properties

Related Categories Alkenyl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents More...
assay   ≥95%
mp   110-113 °C (dec.) (lit.)
SMILES string   [H]\C(CCl)=C(\[H])B(O)O
InChI   1S/C3H6BClO2/c5-3-1-2-4(6)7/h1-2,6-7H,3H2/b2-1+
InChI key   JMTGSXGIIONQHI-OWOJBTEDSA-N

Description

Application

• Reactant for Suzuki-Miyaura cross-coupling reaction

Packaging

1, 5 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 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable
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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