109049-91-4 Usage
Uses
Used in Pharmaceutical Industry:
[2-(2-Oxo-pyrrolidin-1-yl)-phenyl]-acetic acid is used as a cognitive enhancer for its ability to improve cognitive function, memory, and learning. Its neuroprotective properties make it a promising candidate for the treatment of conditions such as Alzheimer's disease and dementia.
Used in Cognitive Enhancement:
[2-(2-Oxo-pyrrolidin-1-yl)-phenyl]-acetic acid is used as a nootropic agent to help individuals seeking to improve their mental performance. Its cognitive-enhancing effects are particularly beneficial for those looking to enhance their memory, learning, and overall cognitive abilities.
Used in Research and Development:
[2-(2-Oxo-pyrrolidin-1-yl)-phenyl]-acetic acid is used as a subject of study in the field of neuroscience and pharmaceutical research. Its potential applications in treating cognitive decline and neurodegenerative diseases make it an important compound for further investigation and development.
Check Digit Verification of cas no
The CAS Registry Mumber 109049-91-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,0,4 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 109049-91:
(8*1)+(7*0)+(6*9)+(5*0)+(4*4)+(3*9)+(2*9)+(1*1)=124
124 % 10 = 4
So 109049-91-4 is a valid CAS Registry Number.
109049-91-4Relevant academic research and scientific papers
SYNTHESIS OF DIHYDRO-1H-PYRROLO- AND TETRAHYDROPYRIDOINDOLES VIA A MODIFIED MADELUNG REACTION
Verboom, W,Orlemans, E.O.M.,Berga, H.J.,Scheltinga, M.W.,Reinhoudt, D.N.
, p. 5053 - 5064 (2007/10/02)
1-(2-Methylphenyl)lactams 9, having different electron -withdrawing groups at the benzylicposition, cyclize under the influence of sodium hydride or potassium tert-butoxyde.Depending on the ring size of the lactam moiety dihydropyrrolo- (10), tetrahydropyridoindole (11), or dihydro-1H-1-benzazepine (12) derivatives are formed.Pyrroloindole 10c has been converted into the corresponding quione 15b.Starting from naphthaleneacetonitrile 20, prepared in 5 steps from 2,3-dichloronaphthoquinone, the 5,10-dioxo-1H-pyrollobenzindole 22 is obtained upon treatment with base and subsequent oxidation of the protected hydroquinone function with ceric ammonium nitrate.
