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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.

The preparation method of the double chlorine sulphur grass amine (by machine translation)

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Paragraph 0014; 0015; 0016; 0018; 0019; 0020, (2017/07/21)

The invention discloses a double-chlorine sulphur grass amine preparation method, which is composed of a 2 - chloro sulfonyl - 7 - fluoro - 5 - ethoxy [1, 2, 4] triazolo [1, 5 - c] pyrimidine in organic solvent with 2, 6 - dichloro the amine passes through condensation reaction; said condensation reaction is 3, 5 - dimethyl pyridine carried out under catalysis. The 2 - chloro sulfonyl - 7 - fluoro - 5 - ethoxy [1, 2, 4] triazolo [1, 5 - c] pyrimidine with the 3, 5 - dimethyl pyridine molar ratio of 1:1 - 1:5. Said organic solvent is dimethyl sulfoxide (DMSO) containing mixed solvent; the mixed solvent of dimethyl sulfoxide in a weight percentage of 0.1% -1%. The method of the invention is high in safety, simple operation, simple process conditions, in particular by selection of appropriate catalyst and organic solvent, can obtain higher reaction yield and purity of the product, is suitable for industrial production. (by machine translation)

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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