17925-97-2 Usage
Uses
Used in Chemical Production:
Benzene, 1-chloro-4-[2,2,2-trichloro-1-(4-Methylphenyl)ethyl]is used as an intermediate in the synthesis of various chemicals and solvents. Its unique structure allows it to be a key component in creating a range of different chemical products.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, Benzene, 1-chloro-4-[2,2,2-trichloro-1-(4-Methylphenyl)ethyl]is utilized as a building block for the development of new drugs. Its specific functional groups and structural features make it a valuable asset in medicinal chemistry.
Used in Agrochemical Production:
Benzene, 1-chloro-4-[2,2,2-trichloro-1-(4-Methylphenyl)ethyl]also finds application in the agrochemical sector, where it is employed in the creation of pesticides and other agricultural chemicals. Its properties contribute to the effectiveness of these products.
Environmental and Health Considerations:
Due to its chlorinated nature, Benzene, 1-chloro-4-[2,2,2-trichloro-1-(4-Methylphenyl)ethyl]may pose risks to the environment and human health. It is crucial to implement proper handling and disposal methods to mitigate any potential harm.
Check Digit Verification of cas no
The CAS Registry Mumber 17925-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,2 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17925-97:
(7*1)+(6*7)+(5*9)+(4*2)+(3*5)+(2*9)+(1*7)=142
142 % 10 = 2
So 17925-97-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H12Cl4/c1-10-2-4-11(5-3-10)14(15(17,18)19)12-6-8-13(16)9-7-12/h2-9,14H,1H3
17925-97-2Relevant academic research and scientific papers
Development of a Panel of Immunoassays for Monitoring DDT, Its Metabolites, and Analogues in Food and Environmental Matrices
Beasley, Helen L.,Phongkham, Thipsavanh,Daunt, Margaret H.,Guihot, Simone L.,Skerritt, John H.
, p. 3339 - 3352 (2007/10/03)
A panel of antisera was prepared using analogues and derivatives of metabolites of the organochlorine insecticide, p,p′-DDT as haptens. The assays developed exhibited differing cross-reactions for different DDT analogues and metabolites, and the choice of
