5287-64-9 Usage
Uses
Used in Pharmaceutical Industry:
5-Keto-D-gluconic acid is used as an intermediate for the synthesis of various pharmaceutical compounds, including antibiotics and antifungal agents. Its unique structure allows for the development of novel drugs with improved efficacy and reduced side effects.
Used in Chemical Industry:
In the chemical industry, 5-Keto-D-gluconic acid is utilized as a building block for the production of various chemicals, such as chelating agents, which are essential for water treatment and metal recovery processes.
Used in Environmental Applications:
5-Keto-D-gluconic acid has potential applications in environmental science, particularly in bioremediation and waste management. Its ability to act as a chelating agent can help in the removal of heavy metals from contaminated sites, thus contributing to environmental sustainability.
Used in Research and Development:
5-Keto-D-gluconic acid serves as an important research tool in the field of biochemistry and molecular biology. It can be used to study the mechanisms of various enzymatic reactions and to develop new methods for the synthesis of complex organic compounds.
Used in Nutritional Supplements:
Due to its role in metabolic processes, 5-Keto-D-gluconic acid may have potential applications in the development of nutritional supplements, particularly for individuals with specific health conditions that require targeted metabolic support.
Check Digit Verification of cas no
The CAS Registry Mumber 5287-64-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,8 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5287-64:
(6*5)+(5*2)+(4*8)+(3*7)+(2*6)+(1*4)=109
109 % 10 = 9
So 5287-64-9 is a valid CAS Registry Number.
5287-64-9Relevant articles and documents
METHOD FOR SELECTIVE CARBOHYDRATE OXIDATION USING SUPPORTED GOLD CATALYSTS
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Page/Page column 40-42, (2010/02/09)
The invention relates to a method for the selective oxidation of a carbohydrate in the presence of a gold catalyst comprising gold particles distributed in a nanodispersed manner on a metal oxide support, and to a method for the selective oxidation of an oligosaccharide in the presence of a gold catalyst comprising gold particles distributed in a nanodispersed manner on a carbon or metal oxide support. The invention also relates to aldonic acid oxidation products produced using said method.
Regio- and stereo-selectivity in homogeneous catalytic hydrogenation of 2,5-diketo-D-threo-hexonic acid
Hamersak, Zdenko,Pavlovic, Nediljko,Delic, Vladimir,Sunjic, Vitomir
, p. 245 - 249 (2007/10/03)
2,5-Diketo-D-threo-hexonic acid (2,5-diketo-D-gluconic acid, 1), a crucial intermediate in the microbial production of L-threo-hex-2-enono-1,4-lactone (L-ascorbic acid, vitamin C), was isolated from the fermentation broth of bacterium Erwinia citreus ATCC 31623, and its regio- and stereo-selective hydrogenation, catalyzed by the water-soluble Ru(II) complex of tris(m-sulfophenyl)phosphine (TPPTS), was performed, The effect of hydrogen pressure, temperature, pH, and catalyst-to-substrate ratio on regio- and stereo-selectivity of the process was studied, at low pH, over 90% regioselectivity in favor of the reduction of the 5-keto group in 1 was achieved, affording L-xylo-2-hexulosonic acid (2-keto-L-gulonic acid, 2) as the main product. Maximal diastereoselectivity, i.e. ratio between 2 and 2-keto-n-gulonic acid (3) expressed as diastereomeric excess (d.e.%), amounted to ca. 50% and was not influenced by any of the above reaction parameters.
