82202-41-3

Usage

Uses

Used in Agriculture:
2,2,2-TRICHLORO-N-PYRIDIN-3-YLACETAMIDE is used as a herbicide for controlling weeds and unwanted plant growth. Its application helps maintain crop productivity and quality by reducing competition from invasive species.
Used in Bactericide Applications:
In addition to its herbicidal properties, 2,2,2-TRICHLORO-N-PYRIDIN-3-YLACETAMIDE is also used as a bactericide, helping to control bacterial infections in crops and prevent yield losses caused by bacterial diseases.
Used in Environmental Management:
Due to its low to moderate persistence in soil and water, 2,2,2-TRICHLORO-N-PYRIDIN-3-YLACETAMIDE is a popular choice for weed control in various agricultural settings, as it minimizes the potential for long-term environmental impact.

InChI:InChI=1/C7H5Cl3N2O/c8-7(9,10)6(13)12-5-2-1-3-11-4-5/h1-4H,(H,12,13)

Upstream product

• 462-08-8 pyridin-3-ylamine 
• 116-16-5 1,1,1,3,3,3-hexachloro-propan-2-one 
• 76-02-8 trifluoroacetyl chloride 

Relevant academic research and scientific papers

BICYCLIC PIPERAZINE COMPOUND AND USE THEREOF

The present invention provides a compound represented by the formula: wherein R1 is an acyl group, R2 is a hydrocarbon group which may be substituted or the like, R3 is a hydrocarbon group which may be substituted or the like, R4 is a hydrocarbon group which may be substituted or the like, n is from 0 to 4, and X is an oxygen atom, a sulfur atom or the like, or a salt thereof. The invention also provides a compound which has a TGR23 antagonist activity and thus is useful for prevention and treatment of cancer.

Formation of N-Substituted Trichloroacetamides from Amines and Hexachloroacetone

Procedures are described for converting primary amines into their well-crystalline trichloroacetyl-derivatives by treatment with hexachloroacetone under mild conditions.Although secondary aromatic N-methylamines are unaffected by hexachloroacetone, saturated heterocyclic amines react vigorously.A mechanistic study using 2-amino-4-t-butylthiazole showed that the reaction is first order in hexachloroacetone, second order in amine, and base-catalysed; there is no appreciable kinetic isotope (H/D) effect nor accumulation of intermediates during the reaction.A sequence which accommodates these results is suggested.