7795-52-0 Usage
Description
(2R)-1-(1H-INDOL-3-YL)PROPAN-2-AMINE, also known as (R)-α-Methyltryptamine, is a chiral compound belonging to the class of indole alkaloids. It is a methylated Tryptamine with a unique stereochemistry, characterized by the presence of a chiral center at the 2-position of the propane amine group. (2R)-1-(1H-INDOL-3-YL)PROPAN-2-AMINE exhibits a range of biological activities and has potential applications in various fields due to its ability to modulate neurotransmitter systems.
Uses
Used in Pharmaceutical Industry:
(2R)-1-(1H-INDOL-3-YL)PROPAN-2-AMINE is used as a pharmaceutical agent for its potential therapeutic applications. As a non-selective serotonin receptor agonist, it acts as a relatively balanced releasing agent of serotonin, norepinephrine, and dopamine. This makes it a promising candidate for the development of drugs targeting various neurological and psychiatric disorders, such as depression, anxiety, and addiction.
Used in Research Applications:
In the field of scientific research, (2R)-1-(1H-INDOL-3-YL)PROPAN-2-AMINE serves as a valuable tool for studying the mechanisms of neurotransmitter release and receptor interactions. Its ability to modulate multiple neurotransmitter systems allows researchers to investigate the complex interplay between these systems and their role in various physiological and pathological processes.
Used in Drug Development:
(2R)-1-(1H-INDOL-3-YL)PROPAN-2-AMINE can be employed as a lead compound in the development of novel drugs with improved efficacy and selectivity. Its unique chemical structure and biological properties provide a foundation for the design of new molecules with tailored pharmacological profiles, potentially leading to the discovery of more effective treatments for various conditions.
Used in Neuropharmacology:
In neuropharmacology, (2R)-1-(1H-INDOL-3-YL)PROPAN-2-AMINE is used to explore the effects of indole alkaloids on the central nervous system. Its ability to act as a psychedelic, stimulant, and entactogenic substance provides insights into the molecular mechanisms underlying these psychoactive effects, which can contribute to the development of safer and more effective psychopharmacological agents.
Overall, (2R)-1-(1H-INDOL-3-YL)PROPAN-2-AMINE is a versatile and promising compound with a wide range of potential applications in various industries, particularly in the pharmaceutical and research sectors. Its unique properties and ability to modulate neurotransmitter systems make it an attractive candidate for further investigation and development.
Check Digit Verification of cas no
The CAS Registry Mumber 7795-52-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,9 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7795-52:
(6*7)+(5*7)+(4*9)+(3*5)+(2*5)+(1*2)=140
140 % 10 = 0
So 7795-52-0 is a valid CAS Registry Number.
7795-52-0Relevant articles and documents
PROCESSES FOR MAKING SERD TRICYCLIC COMPOUNDS HAVING A SUBSTITUTED PHENYL OR PYRIDINYL MOIETY
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, (2022/01/12)
Provided herein are processes for the preparation of compounds useful in the treatment of cancer.
Preparation method of chiral alpha-methyl arylethylamine
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Paragraph 0053; 0056-0076, (2021/06/09)
The invention provides a preparation method of chiral alpha-methyl arylethylamine, and relates to the technical field of organic synthesis medicines. Boc-amino acid methyl ester is used as an initial raw material, Boc-amino alcohol is obtained through reduction, Boc-amino alcohol reacts with thionyl chloride and is oxidized through sodium periodate to obtain a sulfonamide compound, and then the sulfonamide compound is reduced through sodium borohydride promoted by lewis acid and a protecting group is removed under the acidic condition to obtain a target compound. According to the method, raw materials are cheap and easy to obtain, a single optical isomer product is obtained by using chiral raw materials, the problem of column chromatography resolution is solved, generation of a large amount of solid wastes and isomers is avoided, atom economy is improved, the product purity is high, the yield is high, and the production cost is effectively reduced. In addition, the mild reduction system is used for replacing the original high-pressure hydrogenation reaction, the process operation is relatively simple, and the method is more suitable for large-scale industrial production.
METHODS OF TREATING ESTROGEN RECEPTOR-ASSOCIATED DISEASES
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, (2021/09/11)
The present disclosure provides methods of treating estrogen receptor-associated diseases, disorders, and conditions.
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