7460-93-7 Usage
General Description
2,3,4,5-tetrahydroxyhexanenitrile, also known as non-preferred name, is a chemical compound with the molecular formula C6H11NO4. It is a nitrile derivative and contains four hydroxyl groups. 2,3,4,5-tetrahydroxyhexanenitrile (non-preferred name) is primarily used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It also has potential applications in organic synthesis and as a chelating agent in metal ion coordination chemistry. Due to its hydroxyl groups, it can participate in various chemical reactions such as esterification, ether formation, and acylation. However, its non-preferred name suggests that there may be alternative naming conventions for this compound, and it is important to use the correct nomenclature in scientific and industrial applications.
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 articles and documents
Transformation of aldehydes into nitriles in an aqueous medium using O-phenylhydroxylamine as the nitrogen source
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.
