98130-71-3 Usage
Molecular Structure
A chemical compound consisting of a pyrrole ring, an acetic acid moiety, two chlorine atoms at positions 3 and 4, and a 2,5-dihydro-2,5-dioxo group.
Pyrrole Ring
A five-membered aromatic ring with four carbon atoms and one nitrogen atom.
Acetic Acid Moiety
A functional group consisting of a carboxyl group (-COOH) attached to a methyl group (-CH3).
Chlorine Atoms
Two chlorine atoms substituted at positions 3 and 4 of the pyrrole ring, which can influence the compound's reactivity and properties.
2,5-Dihydro-2,5-dioxo Group
A saturated ring structure with two oxygen atoms and a total of five carbon atoms, indicating the presence of a dihydroxyketone group.
Medicinal Chemistry Potential
Pyrrole derivatives, such as 1H-Pyrrole-1-acetic acid, 3,4-dichloro-2,5-dihydro-2,5-dioxo-, are known to exhibit various biological activities, including antimicrobial and antitumor properties.
Reactivity
The presence of chlorine atoms may contribute to the compound's reactivity, making it a potential candidate for organic synthesis.
Further Investigation
The specific uses and properties of 1H-Pyrrole-1-acetic acid, 3,4-dichloro-2,5-dihydro-2,5-dioxo- would need to be explored through experimentation and research to determine its potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 98130-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,1,3 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 98130-71:
(7*9)+(6*8)+(5*1)+(4*3)+(3*0)+(2*7)+(1*1)=143
143 % 10 = 3
So 98130-71-3 is a valid CAS Registry Number.
98130-71-3Relevant academic research and scientific papers
Synthesis and characterization of new compounds containing 1,4-dithiintetracarboxydiimide units
Gǎinǎ, Constantin
, p. 601 - 607 (2007/10/03)
New compounds containing 1,4-dithiintetracarboxydiimide units were synthesized by the disubstitution reaction of N-substituted 2,3- dichloromaleimide with sodium sulflde nonahydrate or thiourea. IR, UV-vis and 1H-NMR spectroscopy, as well as elemental analysis, confirmed their structures. Thermal conversion of 1,4-dithiine ring to thiophene was monitored by differential calorimetry (DSC) and thermogravimetric (TGA) measurements.
