137520-99-1 Usage
Uses
Used in Pharmaceutical Synthesis:
Ethyl 2,6-dichloro-3-methylisonicotinate is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique chemical structure allows it to be a key building block in the creation of new and effective medications.
Used in Agrochemical Development:
In the agrochemical industry, ethyl 2,6-dichloro-3-methylisonicotinate is utilized in the development of new and effective pesticides. Its insecticidal activity against a variety of pests makes it a promising candidate for the formulation of innovative pest control solutions.
Used as an Insecticide:
Ethyl 2,6-dichloro-3-methylisonicotinate is used as an insecticide for its potential to control and eliminate a range of pests. It has been studied for its insecticidal activity, which can contribute to more effective and targeted pest management strategies in agriculture.
Precautionary Note:
While ethyl 2,6-dichloro-3-methylisonicotinate offers significant benefits in its applications, it is important to acknowledge that exposure to this chemical may pose health risks. Therefore, appropriate safety measures and precautions should be taken when handling ethyl 2,6-dichloro-3-methylisonicotinate to minimize any potential adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 137520-99-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,5,2 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137520-99:
(8*1)+(7*3)+(6*7)+(5*5)+(4*2)+(3*0)+(2*9)+(1*9)=131
131 % 10 = 1
So 137520-99-1 is a valid CAS Registry Number.
137520-99-1Relevant academic research and scientific papers
Diels-Alder reactions of 6-alkyl-3,5-dichloro-2H-1,4-oxazin-2-ones with alkynes: Synthesis of 3,5-disubstituted 2,6-dichloropyridines
Meerpoel,Deroover,Van Aken,Lux,Hoornaert
, p. 765 - 768 (2007/10/02)
The Diels-Alder reactiion of 6-alkyl-3,5-dichloro-2H-1,4-oxazin-2-ones 1 with different types of acetylenic compounds 2 is shown to be a versatile method for the generation of variously substituted 2,6-dichloropyridines. In most cases a high degree of reg
