23789-33-5 Usage
Description
ALPHA-FURIL DIOXIME is a chemical compound characterized by its needle-like crystal structure. It exhibits unique chemical properties, being very soluble in alcohol and ether, while slightly soluble in benzene and petroleum ether.
Uses
Used in Chemical Industry:
ALPHA-FURIL DIOXIME is used as a reagent in the alcohol solution for nickel, where it forms an orange-red compound. This application takes advantage of its solubility and chemical reactivity with nickel, making it a valuable component in the chemical industry for specific reactions and processes.
Used in Research and Development:
Due to its unique chemical properties and reactivity, ALPHA-FURIL DIOXIME can also be utilized in research and development for the synthesis of new compounds, studying its interactions with various substances, and potentially discovering new applications in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 23789-33-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,8 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23789-33:
(7*2)+(6*3)+(5*7)+(4*8)+(3*9)+(2*3)+(1*3)=135
135 % 10 = 5
So 23789-33-5 is a valid CAS Registry Number.
23789-33-5Relevant articles and documents
Oxidation of: O -dioxime by (diacetoxyiodo)benzene: Green and mild access to furoxans
He, Chunlin,Pang, Siping,Zhang, Qi,Zhang, Xun,Zhao, Cheng
supporting information, p. 1489 - 1493 (2022/01/31)
Furoxan has been widely used in the field of high energy density materials because of its excellent properties such as high density, high standard enthalpy of formation and high nitrogen content. However, its existing synthesis methods are still restricted by the problems of difficult substrate preparation and manual handling of hazardous reagents. Herein, we disclosed a mild oxidation strategy to efficiently obtain furoxan derivatives starting from readily available o-dioxime substrates. This reaction features high functional group tolerance and easy scale-up, and has excellent regioselectivity for specific nonsymmetric o-dioximes. This method greatly reduces the safety risk and simplifies the operation process, and means that diversified furoxan derivatives can be easily accessed, thus paving the way for the wide application of furoxan derivatives. This journal is
