914458-53-0 Usage
General Description
The chemical compound "(5-bromo-1-pentyl-1H-pyrrol-3-yl)(naphthalen-1-yl)methanone" is a synthetic cannabinoid that belongs to the class of novel psychoactive substances. It is known to have a strong affinity for the cannabinoid receptors in the brain and central nervous system, resulting in potent psychoactive effects when consumed. (5-bromo-1-pentyl-1H-pyrrol-3-yl)(naphthalen-1-yl)methanone has been identified as a designer drug and is often found in products marketed as synthetic marijuana or "legal highs." Due to its potential for abuse and harmful effects on health, it is considered a controlled substance in many jurisdictions and is subject to legal restrictions. The use of "(5-bromo-1-pentyl-1H-pyrrol-3-yl)(naphthalen-1-yl)methanone" can lead to serious health risks, including addiction, psychosis, and cardiovascular complications.
Check Digit Verification of cas no
The CAS Registry Mumber 914458-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,4,5 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 914458-53:
(8*9)+(7*1)+(6*4)+(5*4)+(4*5)+(3*8)+(2*5)+(1*3)=180
180 % 10 = 0
So 914458-53-0 is a valid CAS Registry Number.
914458-53-0Relevant articles and documents
1-Alkyl-2-aryl-4-(1-naphthoyl)pyrroles: New high affinity ligands for the cannabinoid CB1 and CB2 receptors
Huffman, John W.,Padgett, Lea W.,Isherwood, Matthew L.,Wiley, Jenny L.,Martin, Billy R.
, p. 5432 - 5435 (2007/10/03)
Two series of 1-alkyl-2-aryl-4-(1-naphthoyl)pyrroles were synthesized and their affinities for the cannabinoid CB1 and CB2 receptors were determined. In the 2-phenyl series (5) the N-alkyl group was varied from n-propyl to n-heptyl. A second series of 23 1-pentyl-2-aryl-4-(1-naphthoyl)-pyrroles (6) was also prepared. Several compounds in both series have CB1 receptor affinities in the 6-30 nM range. The high affinities of these pyrrole derivatives relative to JWH-030 (1, R = C5H11) support the hypothesis that these pyrroles interact with the CB1 receptor primarily by aromatic stacking.
