6575-04-8 Usage
Uses
Used in Agricultural Industry:
2,4,5-Trichlorobenzonitrile is used as a herbicidal agent for controlling broadleaf and grassy weeds in various crops such as soybeans, cotton, and rice. It functions by inhibiting the process of photosynthesis in plants, which ultimately leads to the death of the weeds. This selective action is crucial for protecting the growth of desired crops while minimizing the impact on the surrounding environment.
The low toxicity to mammals and the lack of bioaccumulation potential of 2,4,5-Trichlorobenzonitrile make it a relatively safer option for agricultural use. However, it is important to note that it may persist in soil and water for extended periods, which necessitates proper handling and disposal procedures to mitigate any potential long-term environmental or health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 6575-04-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6575-04:
(6*6)+(5*5)+(4*7)+(3*5)+(2*0)+(1*4)=108
108 % 10 = 8
So 6575-04-8 is a valid CAS Registry Number.
6575-04-8Relevant academic research and scientific papers
Process for preparing aromatic nitriles
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, (2008/06/13)
Aromatic nitriles having the general formula (I): wherein: - Rrepresents the hydrogen atom., a fluorine, chlorine, bromine or iodine atom, a (C1-C5)-alkoxy group, a carboxy group, a (C1-C5)-carboxy-alkyl, or an aryl group selected from among phenyl, halo-phenyl, phenyl-ether or nitrile; - R' and R"either equal to, or different from, each other, represent the hydrogen atom or a fluorine, chlorine, bromine or iodine atom; are obtained by reacting an organic or inorganic ammonium salt (III):, , NH4(+) X(-) (III), , and an aromatic trichloromethyl derivative having formula (II): wherein R, R' and R" have the above set forth meaning, with the exception that when R in formula (I) represents the nitrile group, the corresponding R group in formula (II) represents the trichloromethyl group, operating in the presence of a catalyst consisting of a metal oxide or a metal salt. The process makes it possible high yields and high selectivities to the useful reaction product to be obtained.
