23627-24-9

Usage

Uses

Used in Agriculture:
2,4,5-TRICHLOROACETANILIDE is used as a herbicide for controlling broadleaf weeds and brush in various crops such as corn, wheat, and tobacco. It is applied as a liquid spray to selectively target and kill unwanted plants by inhibiting their growth processes and protein production, ultimately leading to their death.
Used in Crop Protection:
2,4,5-TRICHLOROACETANILIDE is used as a crop protection agent to ensure the healthy growth of desired crops by eliminating competing weeds and brush. Its selective weed-killing properties make it an effective tool in maintaining crop yields and quality.
However, it is important to note that the use of 2,4,5-TRICHLOROACETANILIDE has been subject to regulatory restrictions and controversy due to concerns about its potential risks to human health and the environment. As a result, its application in agriculture and crop protection may be limited or require careful consideration of alternative methods and products.

InChI:InChI=1/C8H6Cl3NO/c1-4(13)12-8-3-6(10)5(9)2-7(8)11/h2-3H,1H3,(H,12,13)

Upstream product

• 2621-62-7 2,5-dichloroacetanilide 
• 588-07-8 3-Chloroacetanilide 
• 2150-93-8 N-(3,4-dichlorophenyl)acetamide 
• 108-24-7 acetic anhydride 
• 636-30-6 2,4,5-trichloroaniline 
• 64-19-7 acetic acid 
• 90048-73-0 Oxim d. 2,4,5-Trichlor-acetophenons 
• 127-09-3 sodium acetate 
• 7782-50-5 chlorine 
• 75-36-5 acetyl chloride 
• 112160-75-5 acetic acid-(2,5,N-trichloro-anilide) 

Downstream Products

• 40157-48-0 2-nitro-3,4,6-trichloroaniline 
• 609818-66-8 N-(2-nitro-3,4,6-trichlorophenyl)-acetamide 
• 636-30-6 2,4,5-trichloroaniline 
• 37138-82-2 2-methoxy-3,5-dichloronitrobenzene 
• 34283-94-8 2,3,5-trichloronitrobenzene 
• 1086838-05-2 2-nitro-3,4,6-trichlorobenzaldehyde 
• 1086838-06-3 2-bromo-3-nitro-1,4,5-trichlorobenzene 
• 1086838-07-4 3-nitro-1,2,5-trichloro-4-vinylbenzene 
• 15862-07-4 2,4,5-trichlorobiphenyl 

Relevant academic research and scientific papers

ARYLOAZOL-2-YL CYANOETHYLAMINO COMPOUNDS, METHOD OF MAKING AND METHOD OF USING THEREOF

The present invention relates to novel aryloazol-2-yl-cyanoethylamino derivatives of formula (I): wherein R3, R4, R5, R6, R7, P, Q, V, W, X, Y, Z and a are as defined in the description, compositions thereof, processes for their preparation and their uses as pesticides.

ENANTIOMERICALLY ENRICHED ARYLOAZOL-2-YL CYANOETHYLAMINO COMPOUNDS, METHOD OF MAKING AND METHOD OF USING THEREOF

The present invention relates to novel aryloazol-2-yl-cyanoethylamino derivatives substantially enriched in an enantiomer of formula (I): and compounds of formula (IH) wherein R3, R4, R5, R6, R7, R13a, R13b, R14a, R14b, P, Q, V, W, X, Y, Z and a are as defined in the description, compositions thereof, processes for their preparation and their uses as pesticides.

ARYLOAZOL-2-YL CYANOETHYLAMINO COMPOUNDS, METHOD OF MAKING AND METHOD OF USING THEREOF

The present invention relates to novel aryloazol-2-yl-cyanoethylamino derivatives of formula (I):wherein R3, R4, R5, R6, R7, P, Q, V, W, X, Y, Z and a are as defined in the description, compositions thereof, processes for their preparation and their uses as pesticides.

Process for preparing amides by reaction in presence of molecular sieve

There is provided a process for preparing amides which comprises reacting an amine, or an amide, and an acid halide, or anhydride, in suitable molecular proportions, in an inert organic diluent, in the presence of an effective amount of a molecular sieve, until the reaction is completed, separating the molecular sieve, and recovering the amide from the organic mother liquor.

2-(Aminomethyl)phenols, a New Class of Saluretic Agents. 3. Effects of Functional Group Reorientation and Modification

A series of modified 2-(aminomethyl)phenols was synthesized and tested orally in rats for saluretic and diuretic effects.Intravenous dog data are included as supplementary material to show that the diuretic responses, or lack thereof, may be obtained in a second species.Reorientation of the 2-(aminomethyl) group either meta or para to the hydroxyl substituent resulted in loss of diuretic effects.Similarly, replacement of either the phenolic hydroxyl or the aminomethyl group with other functional moieties substantially diminished saluretic effects.