1234370-93-4 Usage
Uses
Used in Pharmaceutical Industry:
(3-Chloro-quinoxalin-2-yl)-isopropyl-amine is used as a potential pharmaceutical agent for its possible biological activity. (3-Chloro-quinoxalin-2-yl)-isopropyl-amine's unique structure, including the quinoxaline ring and the isopropylamine group, may contribute to its interactions with biological targets, offering opportunities for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (3-Chloro-quinoxalin-2-yl)-isopropyl-amine serves as a subject for studying the effects of structural modifications on the properties and reactivity of heterocyclic compounds. Understanding how the isopropylamine group influences the compound's behavior can provide insights into the design of new molecules with tailored properties for various applications.
Further research is necessary to fully understand the properties and potential uses of (3-Chloro-quinoxalin-2-yl)-isopropyl-amine, including its solubility, stability, and interactions with biological systems, which will be crucial for determining its suitability in different industries and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1234370-93-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,4,3,7 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1234370-93:
(9*1)+(8*2)+(7*3)+(6*4)+(5*3)+(4*7)+(3*0)+(2*9)+(1*3)=134
134 % 10 = 4
So 1234370-93-4 is a valid CAS Registry Number.
1234370-93-4Relevant articles and documents
Synthesis of unexpected pyrrolo[2,3- b ]quinoxaline-2-carbaldehydes via sonogashira coupling reaction
Keivanloo, Ali,Bakherad, Mohammad,Rahimi, Amin
experimental part, p. 1599 - 1602 (2010/06/19)
The reaction of a number of N-alkyl-3-chloroquinoxaline-2-amines with propargyl bromide in the presence of PdClPPhand copper(I) iodide in wet morpholine leads to the formation of the unexpected N-substituted pyrrolo[2,3-b]quinoxaline-2-carbaldehydes in good yields. A possible mechanism for the conversion is suggested. Georg Thieme Verlag Stuttgart.
