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145701-21-9

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145701-21-9 Usage

Description

DICLOSULAM is a broad-spectrum, selective herbicide that is specifically designed to control various types of broadleaf weeds and grassy weeds in agricultural crops. It is a potent and effective chemical compound that works by inhibiting the growth and development of weeds, ensuring a healthy and productive crop yield.

Uses

Used in Agriculture:
DICLOSULAM is used as a broadleaf herbicide for controlling a wide range of weeds in various agricultural crops, particularly in soybean and peanut crops. It is applied either preplant or preemergence to maintain maximum control of weed growth, ensuring a healthy and productive crop yield.
Used in Soybean Crops:
In the soybean industry, DICLOSULAM is used as a herbicide to control broadleaf and grassy weeds that can compete with soybean plants for nutrients, water, and sunlight. By effectively controlling these weeds, DICLOSULAM helps to improve the growth and yield of soybean crops.
Used in Peanut Crops:
Similarly, in the peanut industry, DICLOSULAM is used as a herbicide to control weeds that can negatively impact the growth and yield of peanut crops. Its application ensures that peanut plants have the necessary resources to grow and produce a high-quality harvest.

Check Digit Verification of cas no

The CAS Registry Mumber 145701-21-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,7,0 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 145701-21:
(8*1)+(7*4)+(6*5)+(5*7)+(4*0)+(3*1)+(2*2)+(1*1)=109
109 % 10 = 9
So 145701-21-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H10Cl2FN5O3S/c1-2-24-13-17-9(16)6-10-18-12(19-21(10)13)25(22,23)20-11-7(14)4-3-5-8(11)15/h3-6,20H,2H2,1H3

145701-21-9Downstream Products

145701-21-9Relevant articles and documents

HERBICIDAL COMPOSITIONS

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, (2022/03/02)

The present invention provides compositions comprising herbicidally active compounds (A) and (B), where (A) represents one or more compounds of the general formula (I) or agrochemically compatible salts thereof [component (A)], and (B) represents one or more herbicides [component (B)]. The application further relates to a method and to the use of the herbicidal composition according to the invention for controlling harmful plants or for regulating growth.

Preparation method of diclosulam

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Paragraph 0016, (2017/07/22)

The invention provides a preparation method of diclosulam and belongs to the technical field of chemical synthesis. The preparation method comprises the following steps: taking 2,2'-dithio-bis(5-ethyoxyl-7-fluoro[1,2,4]triazole[1,5]pyrimidine) as a raw material, and dropwise adding sulfonyl chloride in the presence of sodium nitrate for carrying out chlorosulfonylation to obtain 2-chlorosulfonyl-5-ethyoxyl-7-fluoro[1,2,4]triazole[1,5]pyrimidine; and carrying out sulfonylation on the 2-chlorosulfonyl-5-ethyoxyl-7-fluoro[1,2,4]triazole[1,5]pyrimidine and 2,6-dichloroaniline in the presence of a catalyst DMAP, so that the diclosulam is obtained. The preparation method provided by the invention has the advantages that the yield and quality are basically consistent with the traditional technology when the diclosulam is obtained by adopting the technology, the problems that usage amount of a highly toxic product chlorine is large and potential safety hazards exist in the traditional technology are solved, the total molar yield reaches more than 80%, and the diclosulam is applicable to industrial production application.

N-ARYLSULFILIMINE COMPOUNDS AND THEIR USE AS CATALYSTS IN THE PREPARATION OF N-ARYLARYLSULFONAMIDE COMPOUNDS

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, (2008/06/13)

N-arylsulfilimine compounds, such as S,S-dimethyl-N-(2,6-dichlorophenyl)sulfilimine, were prepared and found to catalyze the reaction of aromatic sulfonyl chloride compounds, such as 2-chlorosulfonyl-7-fluoro-5-ethoxy[1,2,4]triazolo[1,5-c]pyrimidine, with aromatic amine compounds, such as 2,6-dichloroaniline, to form N-arylarylsulfonamide compounds, such as N-(2,6-dichlorophenyl)-7-fluoro-5-ethoxy[1,2,4]triazolo[1,5-c]-pyrimidine-2-sulfonamide. The aryl moiety of the N-arylsulfilimine catalyst and the aryl moiety of the aromatic amine compound were generally chosen to be identical.

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