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Merck
CN

94735

Vanadyl acetylacetonate

purum, ≥97.0% (RT)

Synonym(s):

VO(acac)2, Vanadium(IV)-oxy acetylacetonate

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About This Item

Linear Formula:
OV(C5H7O2)2
CAS Number:
Molecular Weight:
265.16
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
221-590-8
Beilstein/REAXYS Number:
4138236
MDL number:
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Product Name

Vanadyl acetylacetonate, purum, ≥97.0% (RT)

InChI key

JFHJZWAQYMGNBE-SUKNRPLKSA-L

InChI

1S/2C5H8O2.O.V/c2*1-4(6)3-5(2)7;;/h2*3,6H,1-2H3;;/q;;;+2/p-2/b2*4-3-;;

SMILES string

CC(=O)\C=C(\C)O[V](=O)O\C(C)=C/C(C)=O

grade

purum

assay

≥97.0% (RT)

form

solid

reaction suitability

reagent type: catalyst

mp

235 °C (dec.) (lit.)

Quality Level

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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Marvin W Makinen et al.
The Journal of biological chemistry, 277(14), 12215-12220 (2002-01-30)
We have investigated the interaction of bis(acetylacetonato)oxovanadium(IV) (VO(acac)(2)) with bovine serum albumin (BSA) by EPR and angle-selected electron nuclear double resonance, correlating results with assays of glucose uptake by 3T3-L1 adipocytes. EPR spectra of VO(acac)(2) showed no broadening in the
[Oxidation of phenothiazine and its N-methyl derivative by the combination of iodobenzene and vanadium acetylacetonate].
F Pautet et al.
Die Pharmazie, 40(3), 202-203 (1985-03-01)
N Farrell et al.
Journal of inorganic biochemistry, 30(4), 309-315 (1987-08-01)
A study of the reactions of purine and pyrimidine bases has been initiated with the V(IV) complex [V(O)(acac)2]. Two distinct modes of reaction have been recognized depending on the nature of the base. Simple adduct formation occurs when the base

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