57662-47-2 Usage
Uses
Used in Pharmaceutical Industry:
3-(3-METHYL-1H-INDOL-1-YL)PROPANOIC ACID is used as a sleep aid for its ability to regulate the sleep-wake cycle, helping individuals suffering from sleep disorders, jet lag, and insomnia. Its natural production in the body makes it a preferred choice for those seeking a non-pharmacological approach to improve sleep quality.
Used in Dietary Supplements:
Melatonin is used as a dietary supplement to support overall health and well-being. Its antioxidant properties contribute to the body's defense against oxidative stress and free radicals, potentially reducing the risk of various diseases and promoting a healthy aging process.
Used in Mood Regulation:
3-(3-METHYL-1H-INDOL-1-YL)PROPANOIC ACID is used as a mood regulator due to its neurotransmitter function in the brain. Its potential role in modulating mood and reducing symptoms of depression and anxiety has been the subject of ongoing research.
Used in Immunity Enhancement:
Melatonin is used to enhance the immune system, as it has been shown to possess immunomodulatory properties. Its ability to regulate immune responses and support the body's natural defense mechanisms makes it a valuable component in maintaining overall health.
Used in Neurodegenerative Disease Treatment:
3-(3-METHYL-1H-INDOL-1-YL)PROPANOIC ACID is used as a potential treatment for certain neurodegenerative diseases, such as Alzheimer's and Parkinson's disease. Its antioxidant and neuroprotective properties have been investigated for their potential to slow down the progression of these diseases and improve the quality of life for affected individuals.
Used in Cancer Therapy:
Melatonin is used as a potential therapeutic agent in cancer treatment. Its ability to modulate various cellular processes, such as cell cycle regulation, apoptosis, and angiogenesis, has been studied for its potential to inhibit tumor growth and enhance the effectiveness of conventional cancer therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 57662-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,6 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57662-47:
(7*5)+(6*7)+(5*6)+(4*6)+(3*2)+(2*4)+(1*7)=152
152 % 10 = 2
So 57662-47-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO2/c1-9-8-13(7-6-12(14)15)11-5-3-2-4-10(9)11/h2-5,8H,6-7H2,1H3,(H,14,15)
57662-47-2Relevant academic research and scientific papers
Synthesis of 11-methyl/phenyl-4,5-dihydro-3H-1,4-diazepinoindoles via Bischler-Napieralski type reaction
Basanagoudar, L D,Mahajanshetti, C S,Dambal, S B
, p. 1018 - 1022 (2007/10/02)
A reaction of bromoacetone with N-cyanoethylanilines (1) gives 1-(2-cyanoethyl)-3-methylindoles (3a-d) directly while that of phenacyl bromide and 1 gives the intermediate N-cyanoethyl-N-phenacylanilines (2a-d).Cyclodehydration of 2 with P2O5 in xylene af
269. Intramolecular Carbenoid Reaction of Pyrrole Derivatives. Efficient Syntheses of Pyrrolizinone and Dihydroindolizinone
Jefford, Charles W.,Johncock, William
, p. 2666 - 2671 (2007/10/02)
The copper-catalyzed pyrolysis of 1-diazo-3-(pyrrol-1-yl)-2-propanone (1a) and 1-diazo-4-(pyrrol-1-yl)-2-butanone (1b) in benzene solution gave 1H-pyrrolizin-2-(3H)-one (4a) and 5,6-dihydroindolizin-7(8H)-one (4b), respectively, in quantative yield.Similar pyrolysis of 1-diazo-4-(3-methylindol-1-yl)-2-butanone (9) was less efficient giving 1-methylbenzo-5,6-dihydroindolizin-7(8H)-one (10) and 4-(3-methylindol-1-yl)-but-1-en-3-one (11) in 7percent and 24percent yield, respectively.
Palladium-Assisted N-Alkylation of Indoles: Attempted Application to Polycyclization
Hegedus, Louis S.,Winton, Peter M.,Varaprath Sudarsanan
, p. 2215 - 2221 (2007/10/02)
The palladium(II) complexes of the olefins ethene, propene, and 1-hexene reacted with 1-lithioindole to produce N-alkylated indoles exclusively.Attempts to perform this N-alkylation intramoleculary (to form tricyclic material from 2-allylskatole) failed.Anilines with dienic side chains in the 2-position were subjected to Pd(II)-assisted cyclization conditions in attempts to induce polycyclization.However, only monocyclization was observed.
