89003-76-9 Usage
Uses
Used in Pharmaceutical Industry:
1-(morpholin-4-ylmethyl)-1H-pyrrole-2,5-dione is used as an active pharmaceutical ingredient for the development of antiviral and antibacterial medications. Its potential to inhibit the replication of various viruses, including influenza A and B, as well as certain bacteria, makes it a valuable compound in the formulation of pharmaceuticals aimed at treating viral and bacterial infections.
Used in Antiviral Research:
1-(morpholin-4-ylmethyl)-1H-pyrrole-2,5-dione is used as a research compound for studying its antiviral properties and exploring its potential as a therapeutic agent against viral infections. Its unique molecular structure and pharmacological properties are being investigated to understand its mechanism of action and to develop new antiviral agents based on its chemical structure.
Used in Antibacterial Research:
1-(morpholin-4-ylmethyl)-1H-pyrrole-2,5-dione is also used as a research compound in the field of antibacterial research. Its potential antibacterial properties are being studied to develop new antibacterial agents and to combat antibiotic-resistant bacteria, which is a growing concern in the medical field.
Check Digit Verification of cas no
The CAS Registry Mumber 89003-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,0 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89003-76:
(7*8)+(6*9)+(5*0)+(4*0)+(3*3)+(2*7)+(1*6)=139
139 % 10 = 9
So 89003-76-9 is a valid CAS Registry Number.
89003-76-9Relevant academic research and scientific papers
Synthesis of Diazaheterocycles with a Bridgehead Nitrogen by Photocyclization of N-Substituted Alicyclic Imides
Coyle, John D.,Bryant, Laurence, R. B.
, p. 2857 - 2865 (2007/10/02)
N-(Dialkylaminomethyl)-succinimides or - glutarimides give 1,3-diazabicyclooctanes or --nonanes on irradiation in acetonitrile, accompanied by variable amounts of the parent imide.Two diastereomers of the products can be pbtained, and the relative stereochemistry assigned on the basis of n.m.r. data.With unsymmetrical substrates mixture of products are formed that demonstrate orientational preferences.Analogous N-substituted pyrrolidin-2-ones do not give photocyclised products (an unusual cleavage product is isolated in low yield), and similar dihydrouracils are relatively photostable.N-(Dialkylaminoethyl) aliphatic imides give azepine- or azocine-diones on irradiation, whereas N-(dialkylaminopropyl) compounds undergo photocyclisation to products with a new perhydro-1,4-diazepine ring (as do a corresponding 3,4,5,6-tetrahydrophthalimide and phthalimide, although photoreduction is a major process for the latter system).An N-(dialkylaminobutyl)succinimide does not give products with a new perhydrodiazocine ring.An N-(dialkylaminoethyl)maleimide and the analogous 3,4,5,6-tetrahydrophthalimide give compounds that contain a new piperazine ring, which is in contrast to the saturated imide analogues but similar to the corresponding phthalimide; this process competes effectively with the more usual photoreactions of maleimides involving the carbon-carbon double bond.
