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556580

Sigma-Aldrich

Cyclohexylboronic acid

≥95%

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About This Item

Empirical Formula (Hill Notation):
C6H13BO2
CAS Number:
4441-56-9
Molecular Weight:
127.98
MDL number:
MFCD01311824
UNSPSC Code:
12352103
PubChem Substance ID:
24879564
NACRES:
NA.22

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

Related Categories

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

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Certificates of Analysis (COA)

Lot/Batch Number
SHBP0708
SHBF9628V
SHBD0298V
06396MKV
06396MK

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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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