2580-71-4 Usage
Description
Succinaldehyde dioxime, also known as bis(salicylaldehyde)hydrazone, is a chemical compound with the formula C14H14N4O2. It is a dioxime derivative of succinaldehyde, known for its strong chelating ability due to its two nitrogen atoms. This characteristic allows it to form stable complexes with various transition metal ions, making it a valuable compound in several scientific and industrial applications.
Uses
Used in Analytical Chemistry:
Succinaldehyde dioxime serves as an analytical reagent, utilized for forming complexes with different transition metal ions. Its strong chelating ability aids in the extraction and separation of metal ions from complex mixtures, which is crucial in various analytical processes.
Used in Organic Synthesis:
Due to its chelating properties, succinaldehyde dioxime is employed in organic synthesis. Its ability to form stable complexes with metal ions can facilitate certain reactions or improve the yield of desired products.
Used in Catalysis:
In the field of catalysis, succinaldehyde dioxime is used to enhance the efficiency of catalytic processes. Its metal complexes can act as catalysts or support catalysts, improving the speed and selectivity of chemical reactions.
Used in Electrochemistry:
Succinaldehyde dioxime also finds applications in electrochemistry. The stability of its metal complexes can be advantageous in the development of electrochemical sensors or in processes involving electron transfer.
Check Digit Verification of cas no
The CAS Registry Mumber 2580-71-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2580-71:
(6*2)+(5*5)+(4*8)+(3*0)+(2*7)+(1*1)=84
84 % 10 = 4
So 2580-71-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2O2/c7-5-3-1-2-4-6-8/h3-4,7-8H,1-2H2/b5-3-,6-4-
2580-71-4Relevant articles and documents
1,4-Diaminobutanes from furans: A new synthetic approach to substituted putrescines
Frydman, Benjamin,Ojea, Maria I.
, p. 4765 - 4768 (1998)
A novel approach for the synthesis of (hydroxymethyl)- and (aminomethyl)-putrescines starting with furanmethanols and aminomethyl- furanmethanols is reported. The furans were converted to their 2,5-dimethoxy- tetrahydrofuran derivatives and the latter were ring-opened in acid media. The resulting carbonyl derivatives were isolated as their dioximes and the latter were then reduced to the corresponding amino alcohols.
Green and highly selective protocol for the synthesis of oximes
Ghosh, Pranab,Subba, Raju
, p. 529 - 532 (2013/11/06)
A green and efficient protocol has been developed for the synthesis of either exclusively a monoxime or exclusively a dioxime from a host of 1,2-dicarbonyl compounds on silica.
