191328-21-9 Usage
Description
4-Piperidinecarbonitrile, 4-(2-chlorophenyl)-, also known as 2-(4-[4-(2-chlorophenyl)piperidin-1-yl]butylamino)ethyl benzonitrile, is a chemical compound with the molecular formula C17H21ClN2. It is a piperidine derivative with a carbonitrile group attached to the 4-position of the piperidine ring and a 2-chlorophenyl group attached to the nitrogen atom. This chemical has potential applications in the field of pharmaceuticals and agrochemicals due to its structural features and properties. It may have various biological activities, and further research is being conducted to explore its potential uses in the industry.
Uses
Used in Pharmaceutical Industry:
4-Piperidinecarbonitrile, 4-(2-chlorophenyl)is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structural features and properties make it a promising candidate for the development of new therapeutic agents.
Used in Agrochemical Industry:
4-Piperidinecarbonitrile, 4-(2-chlorophenyl)is used as an agrochemical intermediate for the synthesis of various pesticides and insecticides. Its potential biological activities make it a valuable component in the development of new agrochemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 191328-21-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,3,2 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 191328-21:
(8*1)+(7*9)+(6*1)+(5*3)+(4*2)+(3*8)+(2*2)+(1*1)=129
129 % 10 = 9
So 191328-21-9 is a valid CAS Registry Number.
191328-21-9Relevant articles and documents
Phenylacetamides as selective α-1A adrenergic receptor antagonists
Patane, Michael A.,DiPardo, Robert M.,Newton, Randall C.,Price, RoseAnn P.,Broten, Theodore P.,Chang, Raymond S.L.,Ransom, Richard W.,Di Salvo, Jerry,Nagarathnam, Dhanapalan,Forray, Carlos,Gluchowski, Charles,Bock, Mark G.
, p. 1621 - 1624 (2007/10/03)
A novel class of potent and selective α-1a receptor antagonists has been identified. The structures of these antagonists were derived from truncating the 4-aryl dihydropyridine subunit present in known α-1a antagonists. The design principles which led to the discovery of substituted phenylacetamides, the synthesis and SAR of key analogues, and the results of select in vitro and in vivo studies are described. (C) 2000 Elsevier Science Ltd. All rights reserved.
