96096-68-3 Usage
Description
Pyrrolidine, 1-[2-(3-methoxy-2-nitrophenyl)ethenyl]is a chemical compound with the molecular formula C15H16N2O3. It is an organic compound that contains a pyrrolidine ring and a nitrophenyl group attached to an ethenyl chain. This chemical is commonly used in organic synthesis and medicinal chemistry as a key building block for the development of various pharmaceuticals and bioactive molecules.
Uses
Used in Pharmaceutical Industry:
Pyrrolidine, 1-[2-(3-methoxy-2-nitrophenyl)ethenyl]is used as a key building block for the development of various pharmaceuticals and bioactive molecules. Its unique structure allows for the creation of new drugs with potential applications in treating a wide range of medical conditions.
Used in Drug Discovery:
Pyrrolidine, 1-[2-(3-methoxy-2-nitrophenyl)ethenyl]is used in drug discovery for the treatment of various medical conditions, including cancer, inflammation, and neurological disorders. Its versatile chemical structure enables the design of novel therapeutic agents with improved efficacy and selectivity.
Used in Biological Imaging:
Pyrrolidine, 1-[2-(3-methoxy-2-nitrophenyl)ethenyl]has been studied for its potential function as a fluorescent probe in biological imaging. It has shown promising results for its use in detecting and tracking specific cellular processes, which can aid in the understanding of disease mechanisms and the development of targeted therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 96096-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,0,9 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96096-68:
(7*9)+(6*6)+(5*0)+(4*9)+(3*6)+(2*6)+(1*8)=173
173 % 10 = 3
So 96096-68-3 is a valid CAS Registry Number.
96096-68-3Relevant articles and documents
Psychotomimetic N-Methyl-N-isopropyltryptamines. Effects of Variation of Aromatic Oxygen Substituents
Repke, David B.,Grotjahn, Douglas B.,Shulgin, Alexander T.
, p. 892 - 896 (1985)
Eight N-methyl-N-isopropyltryptamines (MIPTs) possessing various aromatic oxygen substituents were prepared, characterized, and evaluated for hallucinogenic activity in man.In at least two instances (the Ar H and the Ar 5-OCH3, 1 and 4) the unsymmetrical nitrogen substitution led to a substantial increase in potency as well as oral activity when compared to the symmetrical dimethyl homologues.Qualitatively, 4-hydroxy-N-methyl-N-isopropyltryptamine (2) was the most interesting in overall effect, producing a classic hallucinogenic profile.The 5-methoxy congeger 4 resulted in a state characterized by heightened conceptual stimulation lacking in visual phenomena.Other members of the series exhibited diminished effects.
