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521027 Sigma-Aldrich

trans-1-Octen-1-ylboronic acid

≥95%

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

  • CAS Number 42599-16-6

  • Linear Formula CH3(CH2)5CH=CHB(OH)2

  • Molecular Weight 156.03

  •  MDL number MFCD02093734

  •  PubChem Substance ID 24874184

  •  NACRES NA.22

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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   100-104 °C (lit.)
SMILES string   CCCCCC\C=C\B(O)O
InChI   1S/C8H17BO2/c1-2-3-4-5-6-7-8-9(10)11/h7-8,10-11H,2-6H2,1H3/b8-7+
InChI key   RBTAJLKAPFBZDQ-BQYQJAHWSA-N

Description

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

Packaging

1 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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