84596-41-8 Usage
Uses
Used in Pharmaceutical Synthesis:
2-CHLORO-6-(4-CHLOROPHENYL)NICOTINONITRILE is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of biologically active compounds. Its unique structure allows for the creation of new drugs with potential therapeutic benefits.
Used in Agrochemical Production:
In the agrochemical industry, 2-CHLORO-6-(4-CHLOROPHENYL)NICOTINONITRILE serves as an intermediate in the production of various agrochemicals, helping to develop new pesticides or other agricultural chemicals that can improve crop protection and yield.
Used in Medicinal Chemistry Research:
2-CHLORO-6-(4-CHLOROPHENYL)NICOTINONITRILE is utilized in medicinal chemistry research as a building block for the development of new compounds with potential medicinal properties. Its structural features make it a promising candidate for the design and synthesis of novel pharmaceutical agents.
Used in Drug Development:
In the field of drug development, 2-CHLORO-6-(4-CHLOROPHENYL)NICOTINONITRILE plays a role in the discovery and creation of new drug candidates. Its chemical properties and structural attributes are leveraged to enhance the pharmacological potential of emerging therapeutics.
Check Digit Verification of cas no
The CAS Registry Mumber 84596-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,9 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84596-41:
(7*8)+(6*4)+(5*5)+(4*9)+(3*6)+(2*4)+(1*1)=168
168 % 10 = 8
So 84596-41-8 is a valid CAS Registry Number.
84596-41-8Relevant academic research and scientific papers
A facile method for the synthesis of nicotinonitriles from ketones via a one-pot chloromethyleneiminium salt mediated three-component reaction
Asokan,Anabha,Thomas, Ajith Dain,Jose, Ann Maria,Lethesh,Prasanth,Krishanraj
, p. 5641 - 5643 (2008/02/10)
Simple enolizable ketones such as acetophenones and benzalacetones were treated with malononitrile under Vilsmeier-Haack reaction conditions to afford 2-chloronicotinonitriles. The reaction proceeds via a one-pot chloromethyleneiminium salt mediated three
1-Benzoyl-3-(arylphyridyl)urea compounds
-
, (2008/06/13)
The present invention is directed to 1-benzoyl-3-(arylpyridyl)urea compounds useful as insecticides.
