1930-84-3 Usage
Description
3,4-Dichlorophenylisocyanide is an organic compound characterized by the presence of a chlorine atom at both the 3rd and 4th positions of a phenyl ring, with an isocyanide functional group attached. It is known for its reactivity and is commonly utilized in the synthesis of various chemical compounds.
Uses
Used in Chemical Synthesis:
3,4-Dichlorophenylisocyanide is used as a key intermediate in the preparation of N-Dichloro Methylene Aniline compounds. These compounds are significant in the chemical industry due to their potential applications in various fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,4-Dichlorophenylisocyanide is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of molecules with specific biological activities, making it a valuable asset in drug discovery and development.
Used in Agrochemical Industry:
3,4-Dichlorophenylisocyanide also finds application in the agrochemical industry, where it is employed in the synthesis of compounds with pesticidal properties. Its ability to form stable and effective molecules contributes to its importance in this sector.
Check Digit Verification of cas no
The CAS Registry Mumber 1930-84-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,3 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1930-84:
(6*1)+(5*9)+(4*3)+(3*0)+(2*8)+(1*4)=83
83 % 10 = 3
So 1930-84-3 is a valid CAS Registry Number.
1930-84-3Relevant articles and documents
Synthesis and pesticidal properties of thio and seleno analogs of some common urea herbicides
Zakrzewski, Jerzy,Krawczyk, Maria
experimental part, p. 1880 - 1903 (2010/02/28)
Thio and seleno analogs of fenuron, isoproturon, chlorotoluron, metoxuron, monuron, and diuron were synthesized from the corresponding aryl amines. Their reaction with thiophosgene leads to isothiocyanates. Aryl amines were also converted (via isocyanides) to isoselenocyanates. The reaction of both isothio- and isoselenocyanates with dimethylamine affords the corresponding thio and seleno analogs of the above-mentioned urea herbicides. Herbicidal activity of the synthesized compounds was slightly lower than the activity of the parent urea herbicides. The thio and seleno analogs as well as the parent ureas showed good fungicidal activity at a concentration of 200 ppm against selected fungi.
