86702-80-9 Usage
Uses
Used in Agricultural Industry:
Bormoxynil Octanoate is used as a herbicidal agent for the control of broadleaf weeds in various crops. It is particularly effective due to its ability to disrupt the photosynthetic process in unwanted plants, leading to their death. This application helps to protect and enhance crop yields by reducing competition from weeds.
Used in Herbicide Formulations:
Bormoxynil Octanoate is used as a component in herbicide mixtures to broaden the spectrum of weed control and increase the effectiveness of the herbicidal treatment. Its inclusion in these mixtures allows for more comprehensive coverage against a wider range of broadleaf weeds, ensuring a more efficient and targeted approach to weed management in agricultural practices.
Check Digit Verification of cas no
The CAS Registry Mumber 86702-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,0 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86702-80:
(7*8)+(6*6)+(5*7)+(4*0)+(3*2)+(2*8)+(1*0)=149
149 % 10 = 9
So 86702-80-9 is a valid CAS Registry Number.
InChI:InChI=1S/C15H17Br2NO2/c1-2-3-4-5-6-7-14(19)20-15-12(16)8-11(10-18)9-13(15)17/h8-9H,2-7H2,1H3
86702-80-9Relevant academic research and scientific papers
Process for preparing benzonitriles
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, (2008/06/13)
The invention relates to a process for the preparation of a compound of formula I STR1 R is alkyl, and X is bromine or iodine which process comprises: reacting a compound of formula II in a two phase system, said system comprising an aqueous phase and an organic phase comprising a water immiscible solvent, with an acylating agent of formula III or IV in the presence of a base catalyst. STR2
Process for producing esters of 3,5-dibromo-4-hydroxybenzonitrile
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, (2008/06/13)
2,6-dibromo-4-cyanophenyl octanoates and other esters of 3,5-dibromo-4-hydroxybenzonitrile may be produced by reacting 4-hydroxybenzonitrile with bromine in the presence of an inert solvent and catalytic amounts of a basic heterocyclic aromatic compound or its hydrohalide, followed by removal of unreacted bromine and addition of octanoyl chloride or other acyl halide to the reaction mixture and recovery of the desired ester together with recyclable pyridine hydrohalide catalyst and solvent.
