142459-58-3 Usage
Description
Flufenacet is an aromatic amide-based herbicide characterized by its acetamide structure, where the amino hydrogens are replaced by a propan-2-yl and 4-fluorophenyl groups, and the methyl hydrogen is replaced by a [5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl]oxy group. It is specifically designed to control annual grasses and broadleaf weeds in agricultural settings.
Uses
Used in Agricultural Industry:
Flufenacet is used as a pre-emergent herbicide for controlling annual grasses and broadleaf weeds in field corn, corn grown for silage, and soybeans. It is applied to the soil surface or incorporated pre-emergence to effectively manage these types of weeds.
Trade name
AXIOM? Thiafluamide; DOMAIN?;
EPIC?; FOE 5043? technical
Check Digit Verification of cas no
The CAS Registry Mumber 142459-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,4,5 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 142459-58:
(8*1)+(7*4)+(6*2)+(5*4)+(4*5)+(3*9)+(2*5)+(1*8)=133
133 % 10 = 3
So 142459-58-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H13F4N3O2S/c1-8(2)21(10-5-3-9(15)4-6-10)11(22)7-23-13-20-19-12(24-13)14(16,17)18/h3-6,8H,7H2,1-2H3
142459-58-3Relevant 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.
SYNTHESIS METHOD OF THIADIAZOLYLAMIDE DERIVATIVE
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Paragraph 0023, (2015/12/08)
A synthesis method of 2-[(5-(trifluoromethyl)-1,3,4-thiadiazolyl-2-yl)-oxy]amide derivative (I). The method comprises the following step: in a solvent insoluble with water, 2-sulphinyl-5-trifluoromethyl-thiadiazole (II) and amide (III) reacting under the