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20644-97-7

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20644-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20644-97-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,4 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20644-97:
(7*2)+(6*0)+(5*6)+(4*4)+(3*4)+(2*9)+(1*7)=97
97 % 10 = 7
So 20644-97-7 is a valid CAS Registry Number.
InChI:InChI=1/O.V/q;+2/rOV/c1-2/q+2

20644-97-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name oxovanadium(2+)

1.2 Other means of identification

Product number -
Other names Oxovanadium IV

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20644-97-7 SDS

20644-97-7Relevant articles and documents

Dikshitulu, L. S. A.,Chandrasekharam, G.,Rao, V. Hanumantha,Vani, P.

, p. 2455 - 2458 (1981)

Kinetics and mechanisms of the redox reactions of the hydroperoxochromium(III) ion

Wang, Wei-Dong,Bakac, Andreja,Espenson, James H.

, p. 5034 - 5039 (2008/10/08)

The reactions of the hydroperoxochromium(III) ion, (H2O)5CrO2H2+ (CrO2H2+), with Fe2+, VO2+, V2+, Cu+, Ti3+, Co([14]aneN4)2+, Co(Me6[14]aneN4)2+, Co(tim)2+, and [Ru(NH3)6]2+ have been studied in acidic aqueous solution. The reactions are accompanied by large negative entropies of activation, -110 J mol-1 K-1 for Fe2+ and -85 J mol-1 K-1 for Ti3+. All the reactions studied follow an isokinetic relationship in that ΔH? is a linear function of ΔS?. The same is true for the analogous reactions of H2O2. It is proposed that the reactions of CrO2H2+ take place by an inner-sphere, Fenton-type process yielding pentaaquaoxochromium(IV), (H2O)5CrO2+ (CrO2+), as an intermediate. The reactivity of CrO2H2+ as an oxygen transfer reagent is about 20 times greater than that of H2O2. For example, the reactions with (en)2CoSCH2CH2NH22+ to yield (en)2CoS(O)CH2CH2NH22+ have rate constants 20.5 ± 0.4 M-1 s-1 (CrO2H2+) and 1.36 M-1 s-1 (H2O2), both in 0.1 M HClO4 at 25°C. The chromyl ion, CrO2+, oxidizes CrO2H2+ to CrO22+ with a rate constant of (1.34 ± 0.06) × 103 M-1 s-1 in 0.10 M HClO4 in H2O and 266 ± 10 M-1s-1 in D2O.

Kinetics and Mechanism of Oxalic Acid Catalysed Oxidation of Nitrous Acid by Vanadium(V)

Dikshitulu, L. S. A.,Chandrasekharam, G.,Rao, V. Hanumantha,Vani, P.

, p. 150 - 153 (2007/10/02)

The kinetics and mechanism of the oxalic acid catalysed oxidation of nitrous acid by vanadium(V) have been studied in 1 M perchloric acid medium.The reaction is first order each in vanadium(V) and nitrite and fractional order in oxalic acid.Nitrate ion retards the rate of the reaction.At low +>(0.5-1.2 M) the rate of the reaction is independent of +> but at higher concentrations, the rate decreases.Kinetic as well as spectrophotometric evidence for the formation of a 1:1 complex between vanadium(V) and oxalic acid has been obtained and a mechanism involving this complex has been proposed.

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