Skip to Content
Merck
All Photos(1)

Documents

556580

Sigma-Aldrich

Cyclohexylboronic acid

≥95%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C6H13BO2
CAS Number:
Molecular Weight:
127.98
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

Application

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Mirei Shou et al.
Chirality, 27(7), 417-421 (2015-05-23)
Three aldohexoses, glucose, galactose, and mannose, and three aldopentoses, arabinose, xylose, and ribose, were derivatized with L-tryptophanamide (L-TrpNH2 ) under alkaline conditions. Using a basic mobile phase (pH 9.2), the three aldohexoses or the three aldopentoses were simultaneously enantioseparated, respectively, but

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service