19955-83-0 Usage
Uses
Used in Pharmaceutical Industry:
1-(1H-Indol-3-yl)-ethylamine is used as a precursor in the synthesis of various pharmaceutical compounds for its ability to interact with serotonin receptors. This makes it a valuable component in the development of drugs targeting neurological and psychiatric conditions.
Used in Research Applications:
In the scientific community, 1-(1H-Indol-3-yl)-ethylamine is used as a research tool to study the effects of psychoactive substances on the human brain. Its role as a serotonin receptor agonist allows researchers to investigate the mechanisms of action of hallucinogens and other related compounds.
Used in Chemical Synthesis:
1-(1H-Indol-3-yl)-ethylamine is used as a building block in the synthesis of more complex organic molecules. Its versatility in forming a wide range of compounds makes it an essential component in the creation of new chemical entities for various applications, including potential therapeutic uses.
Used in Plant Biology Studies:
As a naturally occurring compound in many plant species, 1-(1H-Indol-3-yl)-ethylamine is used in studies to understand its role in plant physiology and biochemistry. This can provide insights into the production of alkaloids and other secondary metabolites in plants, which may have potential applications in agriculture and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 19955-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,5 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19955-83:
(7*1)+(6*9)+(5*9)+(4*5)+(3*5)+(2*8)+(1*3)=160
160 % 10 = 0
So 19955-83-0 is a valid CAS Registry Number.
19955-83-0Relevant articles and documents
Scope and limitations of reductive amination catalyzed by half-sandwich iridium complexes under mild reaction conditions
Nguyen, Dat P.,Sladek, Rudolph N.,Do, Loi H.
supporting information, (2020/07/15)
The conversion of aldehydes and ketones to 1° amines could be promoted by half-sandwich iridium complexes using ammonium formate as both the nitrogen and hydride source. To optimize this method for green chemical synthesis, we tested various carbonyl substrates in common polar solvents at physiological temperature (37 °C) and ambient pressure. We found that in methanol, excellent selectivity for the amine over alcohol/amide products could be achieved for a broad assortment of carbonyl-containing compounds. In aqueous media, selective reduction of carbonyls to 1° amines was achieved in the absence of acids. Unfortunately, at Ir catalyst concentrations of 1 mM in water, reductive amination efficiency dropped significantly, which suggest that this catalytic methodology might be not suitable for aqueous applications where very low catalyst concentration is required (e.g., inside living cells).
