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2580-71-4

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2580-71-4 Usage

General Description

Succinaldehyde dioxime, also known as bis(salicylaldehyde)hydrazone, is a chemical compound with the formula C14H14N4O2. It is a dioxime derivative of succinaldehyde, and is commonly used as an analytical reagent to form complexes with various transition metal ions. Succinaldehyde dioxime has a strong chelating ability due to its two nitrogen atoms, which allows it to form stable complexes with metal ions, and it is commonly used in the extraction and separation of metal ions from complex mixtures. It also has potential applications in the fields of organic synthesis, catalysis, and electrochemistry due to its chelating properties and stability of its metal complexes.

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-

2580-71-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-hydroxyiminobutylidene)hydroxylamine

1.2 Other means of identification

Product number -
Other names 1,4-Butanedione dioxime

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2580-71-4 SDS

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.

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