15093-84-2 Usage
Molecular Weight
215.25 g/mol
Structure
A pyrrole-2,5-dione derivative with an ethyl and 4-methylphenyl group attached to the pyrrole ring
Organic Synthesis
Used as a building block for the creation of novel organic compounds
Materials Science
Potential use in the development of new materials with specific properties
Pharmaceuticals
Structure shows potential for pharmaceutical applications, but further research is needed
Stability
Stable under normal conditions
Solubility
Soluble in organic solvents such as ethanol, methanol, and acetone
Reactivity
Can undergo various chemical reactions due to the presence of functional groups (e.g., pyrrole-2,5-dione, ethyl, and 4-methylphenyl)
Appearance
Yellow to light brown crystalline solid
Melting Point
Not specified, but typically pyrrole derivatives have moderate to high melting points
Boiling Point
Not specified, but can be estimated based on molecular weight and structure
Density
Not specified, but can be estimated based on molecular weight and structure
Toxicity
Information on toxicity is not provided, but it is important to handle chemicals with caution and follow safety guidelines
Storage
Store in a cool, dry, and well-ventilated area, away from incompatible substances
Disposal
Dispose of according to local regulations and guidelines for chemical waste
Synthesis
ETPT can be synthesized through various methods, such as the reaction of pyrrole-2,5-dione with ethyl and 4-methylphenyl precursors.
Check Digit Verification of cas no
The CAS Registry Mumber 15093-84-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,9 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15093-84:
(7*1)+(6*5)+(5*0)+(4*9)+(3*3)+(2*8)+(1*4)=102
102 % 10 = 2
So 15093-84-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO2/c1-3-14-12(15)8-11(13(14)16)10-6-4-9(2)5-7-10/h4-8H,3H2,1-2H3
15093-84-2Relevant academic research and scientific papers
Weak Coordinating Carboxylate Directed Rhodium(III)-Catalyzed C-H Activation: Switchable Decarboxylative Heck-Type and [4 + 1] Annulation Reactions with Maleimides
Sherikar, Mahadev Sharanappa,Prabhu, Kandikere Ramaiah
supporting information, p. 4525 - 4530 (2019/06/24)
A weakly coordinating carboxylate directing group assisted C-H activation with maleimides leading to novel and switchable decarboxylative Heck-type and [4 + 1] annulation products catalyzed by Rh(III) has been reported. In these reactions, solvents play a
