7460-93-7 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
2,3,4,5-tetrahydroxyhexanenitrile (non-preferred name) is utilized as a key building block in the synthesis of a variety of pharmaceuticals and agrochemicals. Its presence in these industries is attributed to its ability to serve as a versatile intermediate in the creation of complex organic molecules, which can have therapeutic or pesticidal properties.
Used in Organic Synthesis:
In the realm of organic synthesis, 2,3,4,5-tetrahydroxyhexanenitrile (non-preferred name) is employed as a valuable precursor. Its hydroxyl groups facilitate multiple types of chemical reactions, making it a useful component in the assembly of diverse organic compounds.
Used as a Chelating Agent in Metal Ion Coordination Chemistry:
2,3,4,5-tetrahydroxyhexanenitrile (non-preferred name) also finds application as a chelating agent, particularly in metal ion coordination chemistry. The presence of multiple hydroxyl groups enables it to form stable complexes with metal ions, which is crucial in various chemical processes and analytical techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 7460-93-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7460-93:
(6*7)+(5*4)+(4*6)+(3*0)+(2*9)+(1*3)=107
107 % 10 = 7
So 7460-93-7 is a valid CAS Registry Number.
7460-93-7Relevant academic research and scientific papers
Cheewawisuttichai, Thamrongsak,Hurst, Robert D.,Brichacek, Matthew
, (2021)
The conversion of an aldehyde into a nitrile can be efficiently performed using O-phenylhydroxylamine hydrochloride in buffered aqueous solutions. The reported method is specifically optimized for aqueous-soluble substrates including carbohydrates. Several reducing sugars including monosaccharides, disaccharides, and silyl-protected saccharides were transformed into cyanohydrins in high yields. The reaction conditions are also suitable for the formation of nitriles from various types of hydrophobic aldehyde substrates. Furthermore, cyanide can be eliminated from cyanohydrins, analogous to the Wohl degradation, by utilizing a readily-removed weakly basic resin as a promoter.
