17380-74-4 Usage
Description
1-Phenylcyclopentylamine, also known as PCPA, is a chemical compound that belongs to the amphetamine class. It is a potent and selective serotonin releasing agent (SSRA) with potential therapeutic applications in mood disorders and as an antidepressant. PCPA is also a psychoactive drug with stimulant and euphoric effects, although it is not widely available for human consumption and is primarily used in research settings. Its structural similarity to other amphetamine derivatives makes it a valuable subject in medicinal chemistry for the development of new psychoactive drugs with selective serotonin-releasing properties.
Uses
Used in Pharmaceutical Research:
1-Phenylcyclopentylamine is used as a research compound for the development of new psychoactive drugs with selective serotonin-releasing properties. Its unique structure and activity make it a valuable tool in understanding the mechanisms of serotonin release and the potential for treating mood disorders and depression.
Used in Mood Disorder Treatment:
1-Phenylcyclopentylamine is used as a potential treatment for mood disorders due to its potent and selective serotonin releasing action. Its ability to modulate serotonin levels in the brain may offer therapeutic benefits for individuals suffering from mood-related conditions.
Used in Antidepressant Development:
1-Phenylcyclopentylamine is used as a potential antidepressant, leveraging its SSRA properties to alleviate symptoms of depression. 1-Phenylcyclopentylamine's ability to release serotonin selectively may provide a more targeted approach to treating depressive disorders compared to traditional antidepressants.
Used in Recreational Drug Use:
Although not widely available for human consumption, 1-Phenylcyclopentylamine has been used recreationally due to its stimulant and euphoric effects. Its psychoactive properties have garnered interest among some individuals seeking altered states of consciousness or enhanced mood experiences. However, the recreational use of PCPA is not recommended due to potential health risks and legal implications.
Check Digit Verification of cas no
The CAS Registry Mumber 17380-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,8 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17380-74:
(7*1)+(6*7)+(5*3)+(4*8)+(3*0)+(2*7)+(1*4)=114
114 % 10 = 4
So 17380-74-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H15N/c12-11(8-4-5-9-11)10-6-2-1-3-7-10/h1-3,6-7H,4-5,8-9,12H2
17380-74-4Relevant articles and documents
-
Balderman,D.,Kalir,A.
, p. 24 - 26 (1978)
-
DIARYLALKYLAMINE REV-ERB ANTAGONISTS AND THEIR USE AS MEDICAMENTS
-
Page/Page column 48; 63; 71, (2015/04/28)
The present invention relates to compounds of Formula (I) or pharmaceutically acceptable salts or solvates thereof : It further discloses a pharmaceutical composition comprising the compounds of Formula (I) and their uses as anti-proliferative and pro-apoptotic agents for cancer therapy.
A modified Curtius reaction: an efficient and simple method for direct isolation of free amine
Ma, Bin,Lee, Wen-Cherng
experimental part, p. 385 - 386 (2010/03/03)
The Curtius rearrangement and related reactions are often used to convert carboxylic acids to the corresponding primary amines. However, this reaction often requires harsh conditions for hydrolysis of the isocyanate intermediates to amines, and can also be contaminated by the formation of corresponding ureas due to the reactive nature of the intermediates. We have discovered that by quenching the isocyanate intermediates with sodium trimethylsilanolate, the free amines can be isolated after aqueous workup. This mild and fast procedure provides free amines in one pot with good yields.