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Merck
CN

556580

Cyclohexylboronic acid

≥95%

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About This Item

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

Cyclohexylboronic acid, ≥95%

InChI

1S/C6H13BO2/c8-7(9)6-4-2-1-3-5-6/h6,8-9H,1-5H2

SMILES string

OB(O)C1CCCCC1

InChI key

XDRVAZAFNWDVOE-UHFFFAOYSA-N

assay

≥95%

form

powder

Quality Level

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

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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

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