162934-76-1 Usage
Description
Naphthalen-1-yl(1H-pyrrol-3-yl)methanone is an organic compound characterized by its brown foam appearance. It is known for its unique chemical structure that features a naphthalene ring connected to a pyrrole ring through a methylene bridge. naphthalen-1-yl(1H-pyrrol-3-yl)methanone is of interest in the field of medicinal chemistry due to its potential interactions with biological targets.
Uses
Used in Pharmaceutical Industry:
Naphthalen-1-yl(1H-pyrrol-3-yl)methanone is used as a key intermediate in the synthesis of high affinity ligands for the cannabinoid CB1 and CB2 receptors. These ligands are crucial for developing new drugs targeting these receptors, which play a significant role in various physiological processes, including pain, appetite, and immune response regulation. The development of such ligands can lead to innovative treatments for a range of conditions, including chronic pain, obesity, and inflammatory diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 162934-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,9,3 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 162934-76:
(8*1)+(7*6)+(6*2)+(5*9)+(4*3)+(3*4)+(2*7)+(1*6)=151
151 % 10 = 1
So 162934-76-1 is a valid CAS Registry Number.
162934-76-1Relevant articles and documents
Imidazole derivatives having an inhibitory activity for farnesyl transferase and process for preparation thereof
-
, (2008/06/13)
The present invention relates to a novel imidazole derivative represented by formula (1) which shows an inhibitory activity against farnesyl transferase or pharmaceutically acceptable salts or isomers thereof, in which A, n1and Y are defined in the specification; to a process for preparation of the compound of formula (1); to intermediates which are used in the preparation of the compound of formula (1); and to a pharmaceutical composition comprising the compound of formula (1) as an active ingredient.
The regioselective photoinduced aroylation at the 3-position of pyrrole derivatives
Oda, Kazuaki,Hiratsuka, Rin,Machida, Minoru
, p. 463 - 470 (2007/10/03)
Irradiation of arenecarbothioamide with pyrrole or indole derivatives gave regioselectively 3-aroylpyrrole or -indole derivatives, respectively.