18585-06-3 Usage
Uses
Used in Agrochemical Industry:
ETHYL 4-CHLORO-3-TRIFLUOROMETHYLCARBANILATE is used as an active ingredient in the production of pesticides for its strong insecticidal and fungicidal properties. It helps protect crops from pests and diseases, ensuring higher yields and better quality produce.
Used in Pharmaceutical Industry:
ETHYL 4-CHLORO-3-TRIFLUOROMETHYLCARBANILATE is used as an intermediate in the synthesis of various pharmaceuticals. Its ability to inhibit the growth of certain bacteria and fungi makes it a valuable component in the development of drugs targeting specific infections and diseases.
Safety Precautions:
ETHYL 4-CHLORO-3-TRIFLUOROMETHYLCARBANILATE is hazardous if ingested or inhaled. It should be handled with care in a well-ventilated area and with appropriate protective equipment to minimize the risk of exposure. Proper storage and disposal methods should be followed to ensure the safety of workers and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 18585-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,8 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18585-06:
(7*1)+(6*8)+(5*5)+(4*8)+(3*5)+(2*0)+(1*6)=133
133 % 10 = 3
So 18585-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClF3NO2/c1-2-17-9(16)15-6-3-4-8(11)7(5-6)10(12,13)14/h3-5H,2H2,1H3,(H,15,16)
18585-06-3Relevant academic research and scientific papers
Teaching Old Compounds New Tricks: DDQ-Photocatalyzed C?H Amination of Arenes with Carbamates, Urea, and N-Heterocycles
Das, Somnath,Natarajan, Palani,K?nig, Burkhard
supporting information, p. 18161 - 18165 (2017/12/28)
The C?H amination of benzene derivatives was achieved using DDQ as photocatalyst and BocNH2 as the amine source under aerobic conditions and visible light irradiation. Electron-deficient and electron-rich benzenes react as substrates with moderate to good product yields. The amine scope of the reaction comprises Boc-amine, carbamates, pyrazoles, sulfonimides and urea. Preliminary mechanistic investigations indicate arene oxidation by the triplet of DDQ to radical cations with different electrophilicity and a charge transfer complex between the amine and DDQ as intermediate of the reaction.
