68350-65-2 Usage
Nitrile derivative
2-(3-chloroquinoxalin-2-yl)acetonitrile is derived from 3-chloroquinoxaline by replacing a hydrogen atom with a cyano group (CN).
Common use
Intermediate in the synthesis of pharmaceuticals and agrochemicals 2-(3-chloroquinoxalin-2-yl)acetonitrile is widely used as a starting material for creating various medicinal and chemical products.
Potential biological activities
2-(3-chloroquinoxalin-2-yl)acetonitrile has shown possible biological effects, making it a candidate for further research and development in drug creation.
Organic synthesis building block
The compound serves as a fundamental component in preparing complex organic molecules, which can be used in various applications.
Medicinal chemistry application
Development of novel therapeutic agents 2-(3-chloroquinoxalin-2-yl)acetonitrile is utilized in the creation of new drugs and treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 68350-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,5 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68350-65:
(7*6)+(6*8)+(5*3)+(4*5)+(3*0)+(2*6)+(1*5)=142
142 % 10 = 2
So 68350-65-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H6ClN3/c11-10-9(5-6-12)13-7-3-1-2-4-8(7)14-10/h1-4H,5H2
68350-65-2Relevant academic research and scientific papers
Synthesis and Some Reactions of 3-Chloro-2-(cyanomethylene)-1,2-dihydroquinoxalines
Obefami, Craig A.,Pfleiderer, Wolfgang
, p. 223 - 231 (2007/10/03)
2,3-Dichloroquinoxaline and some of its derivatives have been reacted with malononitrile and ethyl cyanoacetate to yield a variety of 3-chloro-2-(cyanomethylene)-1,2-dihydroquinoxaline derivatives. The reaction of 3-chloro-2-(dicyanomethylene)-1,2-dihydroquinoxaline (2e) with pyridine and its methyl derivatives led to the zwitterionic structures 6a-c. The structures of the newly synthesized compounds were assigned by spectroscopic data and elemental analyses.
