5358-06-5 Usage
Uses
Used in Agricultural Applications:
Methyl 2,3,4,5-tetrachloro-6-cyanobenzoate is used as a pesticide or herbicide for [application reason]. Its effectiveness in controlling pests and unwanted plant growth is attributed to its chemical properties, which allow it to target and eliminate the organisms that interfere with crop production.
Used in Chemical Research:
In the field of chemical research, methyl 2,3,4,5-tetrachloro-6-cyanobenzoate is used as a compound for [application reason], such as studying its chemical behavior, interactions with other substances, and potential applications in various chemical processes.
Used in Industrial Chemical Production:
Methyl 2,3,4,5-tetrachloro-6-cyanobenzoate is utilized as an intermediate or component in the production of various industrial chemicals for [application reason]. Its unique properties make it a valuable contributor to the synthesis of other compounds used in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5358-06-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5358-06:
(6*5)+(5*3)+(4*5)+(3*8)+(2*0)+(1*6)=95
95 % 10 = 5
So 5358-06-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H3Cl4NO2/c1-16-9(15)4-3(2-14)5(10)7(12)8(13)6(4)11/h1H3
5358-06-5Relevant academic research and scientific papers
ISOINDOLINONE PIGMENTS AND A METHOD OF MANUFACTURING.
-
Page/Page column 14-15, (2008/12/08)
An isoindolinone pigment having hexachlorobenzene (HCB) content less than 10 ppm and a method of manfacturing.
Process for the preparation of alkyl esters of tetrachloro-2-cyano-benzoic acid
-
, (2008/06/13)
Tetrachloro-2-cyanobenzoic acid alkyl esters of formula STR1 wherein R is C1 -C5 alkyl, can be very conveniently prepared by (a) reacting the ammonium salt of tetrachloro-2-cyanobenzoic acid, in the presence of water and an inert organic solvent, with a hydroxide of formula MOH, wherein M is Na or K, and removing the ammonia evolved, and (b) reacting the resultant salt of the formula STR2 wherein M is as defined above, with at least 1 mole of a dialkyl sulfate of formula SO2 (OR)2 or an alkyl halide of formula RHal, wherein R is as defined above and Hal is Cl, Br, I or F, also in the presence of water and an inert organic solvent.
