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56257

Supelco

Ferroceneboronic acid

LiChropur, ≥97.0% (HPLC)

Synonym(s):

(Boronocyclopentadienyl)cyclopentadienyl iron, NSC 119337

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About This Item

Empirical Formula (Hill Notation):
C10H11BFeO2
CAS Number:
Molecular Weight:
229.85
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22

grade

derivatization grade ((HPLC))

Quality Level

assay

≥97.0% (HPLC)

quality

LiChropur

reaction suitability

reagent type: catalyst
core: iron

technique(s)

HPLC: suitable

mp

145-150 °C (dec.) (lit.)

SMILES string

[Fe].[CH]1[CH][CH][CH][CH]1.OB(O)[C]2[CH][CH][CH][CH]2

InChI

1S/C5H6BO2.C5H5.Fe/c7-6(8)5-3-1-2-4-5;1-2-4-5-3-1;/h1-4,7-8H;1-5H;

InChI key

HHGAJIKAUQWFKH-UHFFFAOYSA-N

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Application

Derivatization reagent for the determination of brassinosteroids[1]
Redox-acitce electrochemical probe to monitor interactions involving sugars

Reactant involved in:
  • Synthesis of ferrocene-appended subporphyrins for electrochemical property studies
  • Synthesis of catalysts for polymerization of olefins
  • Suzuki-coupling reaction with organic triflates
  • Catalytic ortho-lithiation

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Contains varying amounts of anhydride

Recommended products

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Interactions of select boric acid derivatives with β-cyclodextrin were investigated. All products were obtained employing the grinding-induced mechanochemical approach. It was found that phenylboronic acid, benzoxaborole and boric acid form non-covalent, hydrogen bonding-based systems with β-cyclodextrin, whereas catechol and pinacol

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