96740-32-8 Usage
Description
METHYL PARATHION-D6 is a derivative of Parathion, an organophosphate insecticide commonly used in agriculture for pest control. It is characterized by its ability to target and eliminate a wide range of pests, making it a valuable tool in protecting crops.
Uses
Used in Agriculture:
METHYL PARATHION-D6 is used as an insecticide for controlling pests in various crops such as cotton, rice, and fruit trees. Its application helps to protect these plants from damage caused by insects, ensuring a healthy and productive yield.
Used in Cotton Production:
In the cotton industry, METHYL PARATHION-D6 is used as a pesticide to eliminate pests that can damage the cotton plants and reduce the quality of the cotton fibers. This helps to maintain the integrity and value of the cotton crop.
Used in Rice Cultivation:
METHYL PARATHION-D6 is utilized in rice farming to control insect infestations that can threaten the growth and productivity of rice plants. By managing these pests, rice farmers can ensure a stable and abundant harvest.
Used in Fruit Tree Cultivation:
For fruit tree growers, METHYL PARATHION-D6 serves as an essential tool in managing insect populations that can harm the trees and reduce fruit production. Its application helps to protect the health of the trees and the quality of the fruit they produce.
Check Digit Verification of cas no
The CAS Registry Mumber 96740-32-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,4 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 96740-32:
(7*9)+(6*6)+(5*7)+(4*4)+(3*0)+(2*3)+(1*2)=158
158 % 10 = 8
So 96740-32-8 is a valid CAS Registry Number.
96740-32-8Relevant articles and documents
Preparation method of deuterated methyl parathion
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Paragraph 0039; 0046-0049; 0050; 0059, (2018/12/02)
The invention discloses a preparation method of deuterated methyl parathion. The preparation method comprises the following steps: (1) performing the mono-esterification for thiophosphoryl chloride and deuterated methanol, and obtaining a reaction product