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556580 Sigma-Aldrich

Cyclohexylboronic acid

≥95%

  • CAS Number 4441-56-9

  • Empirical Formula (Hill Notation) C6H13BO2

  • Molecular Weight 127.98

  •  MDL number MFCD01311824

  •  PubChem Substance ID 24879564

  •  NACRES NA.22

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Properties

Related Categories Alkyl and Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents More...
assay   ≥95%
form   powder
SMILES string   OB(O)C1CCCCC1
InChI   1S/C6H13BO2/c8-7(9)6-4-2-1-3-5-6/h6,8-9H,1-5H2
InChI key   XDRVAZAFNWDVOE-UHFFFAOYSA-N

Description

Application

Reactant involved in:
• HF-free synthesis of tetrabutylammonium trifluoroborates
• Cross-coupling with aromatic amines
• Suzuki cross-coupling reactions
• Arylation and alkylation of diphenylisoxazole

Packaging

5, 10 g in glass bottle

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
RTECS 
GU7171000
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Certificate of Origin (COO)

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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

Peer-Reviewed Papers
15

References

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