58131-47-8 Usage
Uses
Used in Pharmaceutical Industry:
Methanesulfonic acid calcium salt is used as a reagent in the synthesis of pharmaceuticals for its ability to facilitate specific chemical reactions, contributing to the production of various medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, methanesulfonic acid calcium salt is utilized as a reagent in the synthesis of agrochemicals, aiding in the creation of substances that support agricultural processes and crop protection.
Used as an Acid Catalyst in Organic Synthesis:
Methanesulfonic acid calcium salt is employed as an acid catalyst in organic synthesis, enabling specific reactions to proceed more efficiently and selectively, which is crucial for the production of a wide range of chemical products.
Used as an Environmentally Friendly Alternative to Strong Acids:
Recognized for its safety and reduced environmental impact, methanesulfonic acid calcium salt is used as a substitute for traditional strong acids like sulfuric acid and hydrochloric acid, minimizing hazards and environmental pollution associated with their use.
Check Digit Verification of cas no
The CAS Registry Mumber 58131-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,3 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58131-47:
(7*5)+(6*8)+(5*1)+(4*3)+(3*1)+(2*4)+(1*7)=118
118 % 10 = 8
So 58131-47-8 is a valid CAS Registry Number.
58131-47-8Relevant academic research and scientific papers
Thermal Analysis Study of Phase Transformations of Magnesium and Calcium Methanesulfonates
Kosova, D. A.,Kuzovchikov, S. V.,Provotorov, D. I.,Uspenskaya, I. A.
, p. 752 - 757 (2020/06/18)
Abstract: Anhydrous magnesium methanesulfonate (Mg(SO3CH3)2) and calcium methanesulfonate (Ca(SO3CH3)2) as well as hydrates Mg(SO3CH3)2 · 2H2O an
Lanthanide replacement in organic synthesis: Luche-type reduction of α,β-unsaturated ketones in the presence of calcium triflate
Forkel, Nina V.,Henderson, David A.,Fuchter, Matthew J.
supporting information; experimental part, p. 2129 - 2132 (2012/09/08)
Development of a calcium-mediated regioselective 1,2-reduction of challenging α,β-unsaturated ketones, such as 2-cyclopententone, is reported. The corresponding allylic alcohols are obtained in very good regioselectivities using Ca(OTf)2 and NaBH4. Furthermore, we have shown that our method can stereoselectively reduce aziridinyl ketones.
