14217-01-7 Usage
Uses
Used in Laboratory Applications:
Chromic potassium oxalate is used as an oxidizing agent in various laboratory experiments and procedures, due to its strong oxidizing properties.
Used in Dye and Pigment Production:
Chromic potassium oxalate is used in the production of dyes and pigments, contributing to the vibrant colors and stability of these products.
Used in Tanning Industry:
In the tanning industry, chromic potassium oxalate is used as a tanning agent, helping to preserve and color leather.
Used in Safety Matches Production:
Chromic potassium oxalate is used in the manufacture of safety matches, providing the necessary oxidizing properties for the match heads to ignite.
Used in Photography:
In the field of photography, chromic potassium oxalate is used in certain processes, such as the development of film or prints.
Used as a Corrosion Inhibitor:
Chromic potassium oxalate is used as a corrosion inhibitor in various industrial applications, helping to protect metal surfaces from corrosion and wear.
Check Digit Verification of cas no
The CAS Registry Mumber 14217-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,1 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14217-01:
(7*1)+(6*4)+(5*2)+(4*1)+(3*7)+(2*0)+(1*1)=67
67 % 10 = 7
So 14217-01-7 is a valid CAS Registry Number.
InChI:InChI=1/3C2H2O4.Cr/c3*3-1(4)2(5)6;/h3*(H,3,4)(H,5,6);
14217-01-7Relevant academic research and scientific papers
Application of the Pfeiffer effect to the assignment of absolute configurations to octahedral metal complexes of the type cis-[M(diamine)2(X)(Y)]n+ and related complexes
Miyoshi, Katsuhiko,Matsumoto, Yuuko,Yoneda, Hayami
, p. 1057 - 1062 (2008/10/08)
The Pfeiffer effect of [Cr(ox)3]3- (ox = oxalate dianion) was examined by using as a chiral environment substance optically stable metal complexes of the type cis-[M(diamine)2(X)(Y)]n+ (M = Co3+ or Cr3+, diamine = ethylenediamine (en) or trimethylenediamine (tn), and X and/or Y = anionic monodentate ligand) and their related complexes in dioxane-water mixtures. It was found that the chiral equilibrium of [Cr(ox)3]3- is always displaced in favor of its Δ enantiomer in the presence of Λ enantiomers of these complexes added as an environment substance. This was interpreted to mean that Λ-cis-[M(diamine)2(X)(Y)]n+ complexes associate more preferably with Δ-[Cr(ox)3]3- than with its antipode, the inversion rate of Δ-[Cr(ox)3]3- being thereby retarded relative to that of the antipode. On the basis of this finding, it was proposed that the absolute configuration of cis-[M(en or tn)2(X)(Y)]n+ and of the related complexes is inferred from the direction of the equilibrium shift in racemic [Cr(ox)3]3- induced by these chiral complexes. An association model was also proposed for the stereoselective interaction between cis-[M(diamine)2(X)(Y)]n+ and [Cr(ox)3]3-.
