3741-24-0 Usage
Uses
Due to the limited information available on (1,1-Bipyrrolidine)-2,2,5,5-tetrone, the following uses are speculative and based on the general properties of tetrone compounds and pyrrolidines:
Used in Organic Synthesis:
(1,1-Bipyrrolidine)-2,2,5,5-tetrone is used as a synthetic intermediate for the development of various organic compounds. Its unique structure, which includes a four-membered cyclic ester and a nitrogen atom, allows it to participate in a range of chemical reactions, facilitating the synthesis of complex organic molecules.
Used in Pharmaceutical Development:
As a member of the tetrone and pyrrolidine groups, (1,1-Bipyrrolidine)-2,2,5,5-tetrone may be used as a building block in the design and synthesis of new pharmaceutical agents. Its potential role in drug discovery could be attributed to its ability to form stable complexes with biological targets, contributing to the development of novel therapeutics.
Used in Chemical Research:
(1,1-Bipyrrolidine)-2,2,5,5-tetrone could be utilized in academic and industrial research settings to study the properties of tetrone compounds and their interactions with other chemical entities. This research could lead to a better understanding of the compound's reactivity, stability, and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 3741-24-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,4 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3741-24:
(6*3)+(5*7)+(4*4)+(3*1)+(2*2)+(1*4)=80
80 % 10 = 0
So 3741-24-0 is a valid CAS Registry Number.
3741-24-0Relevant academic research and scientific papers
One-step ring condensation of hydrazine derivatives and cyclic anhydrides
Katrusiak, Anna,Katrusiak, Andrzej
, p. 28 - 36 (2015/03/05)
Hydroxypyridazinone and pyrroledione rings condensation in the reactions of hydrazine hydrate with citraconic, 2,3-dimethylmaleic, succinic and cis-cyclohexanedicarboxylic anhydrides have been conducted in the HCl aqueous solution. The pyridazine-ring condensation yields products unexpected for these conditions. They have been identified by 1H/13C NMR and X-ray diffraction. The course of the reaction toward the five- and six-membered ring condensation strongly depends on methyl and other substituents in the anhydrides and in hydrazine. The obtained products indicate that the ring condensation is controlled by the molecular strains and steric hindrances between the substituents in anhydrides and pyridazinone products. The condensation of cyclic anhydrides with hydrazines has been reduced to one-step reaction and its yield significantly increased.
