52986-66-0 Usage
Uses
Used in Pesticide Industry:
2-(CHLOROMETHYL)PHENYL ISOCYANATE is used as a key intermediate in the synthesis of various pesticides. Its high reactivity allows for the production of effective compounds that protect crops from pests and diseases, contributing to increased agricultural productivity.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-(CHLOROMETHYL)PHENYL ISOCYANATE serves as a crucial building block for the development of new drugs. Its unique chemical properties enable the creation of innovative therapeutic agents that address various health conditions and diseases.
Used in Industrial Chemicals Production:
2-(CHLOROMETHYL)PHENYL ISOCYANATE is also utilized in the manufacturing of other industrial chemicals. Its versatility and reactivity make it a valuable component in the synthesis of a wide range of chemical products used in various industries, such as plastics, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 52986-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,9,8 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52986-66:
(7*5)+(6*2)+(5*9)+(4*8)+(3*6)+(2*6)+(1*6)=160
160 % 10 = 0
So 52986-66-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClNO/c9-5-7-3-1-2-4-8(7)10-6-11/h1-4H,5H2
52986-66-0Relevant academic research and scientific papers
Process for the preparation of 1-aminoanthraquinone
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, (2008/06/13)
A process for preparing 1-aminoanthraquinone, comprising the steps of: A. reacting o-chloromethylphenylisocyanate with at least an equivalent amount of benzene in anhydrous hydrofluoric acid at a temperature of about -10° to 200° C to form the lactam of 2-amino-diphenylmethane-2'-carboxylic acid, B. saponifying the lactam of 2-amino-diphenylmethane-2'-carboxylic acid with aqueous alkali at a temperature above about 100° C to form the 2-amino-diphenylmethane-2'-carboxylic acid, C. contacting the 2-amino-diphenylmethane-2'-carboxylic acid with an acid condensation agent, thereby to convert the carboxylic acid to 4-amino-anthrone, and D. contacting the 4-aminoanthrone with an oxidizing agent in an acid or alkaline medium, thereby to convert the aminoanthrone to 1-aminoanthraquinone. Special conditions are also recited for carrying out the individual steps to obtain high yields.
