6063-67-8 Usage
Uses
Used in Medicinal Chemistry:
(2Z)-N-(3-bromophenyl)-2-cyano-3-[4-(dimethylamino)phenyl]prop-2-enamide is used as a compound in medicinal chemistry for its potential to be developed into pharmaceutical agents. Its unique structural features, including the presence of a cyanide group, a bromine atom, and a dimethylamino group, may offer opportunities for the design of new drugs with specific therapeutic properties.
Used in Drug Development:
In the field of drug development, (2Z)-N-(3-bromophenyl)-2-cyano-3-[4-(dimethylamino)phenyl]prop-2-enamide is utilized as a starting material or intermediate in the synthesis of new pharmaceuticals. Its structural components may allow for the creation of molecules with targeted biological activities, making it a valuable asset in the search for novel therapeutic agents.
It is crucial to handle (2Z)-N-(3-bromophenyl)-2-cyano-3-[4-(dimethylamino)phenyl]prop-2-enamide with care and follow safety protocols, as it may present risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 6063-67-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6063-67:
(6*6)+(5*0)+(4*6)+(3*3)+(2*6)+(1*7)=88
88 % 10 = 8
So 6063-67-8 is a valid CAS Registry Number.
6063-67-8Relevant academic research and scientific papers
Boron-nitrogen compounds. XXV. Substituted 1,3,2-diazaboracycloalkanes
Weber, Wolfgang,Dawson, John W.,Niedenzu, Kurt
, p. 726 - 728 (2008/10/08)
Boron- and nitrogen-substituted 1,3,2-diazaboracycloalkanes have been prepared by a transamination between bis(dimethylamino)boranes and α,ω-diamines. Partial substitution of the nitrogen of the diamine does not appear to inhibit this reaction; five-, six-, and seven-membered heterocyclic systems are readily obtained by the described procedure. However, the low yields of product obtained in those reactions involving an olefinic α,ω-diamine indicate that steric factors may play an important role. The mechanism of the formation of the boron-nitrogen-carbon heterocycles is discussed, and some spectroscopic data are briefly evaluated.
