23627-24-9

Basic information

• Product Name: 2,4,5-TRICHLOROACETANILIDE
• Synonyms: 2,4,5-trichlorophenylacetamide;2’,4’,5’-trichloro-acetanilid;Acetamide, N-(2,4,5-trichlorophenyl)-;N-(2,4,5-Trichlorophenyl)acetamide;2',4',5'-TRICHLOROACETANILIDE;2,4,5-TRICHLOROACETANILIDE;2'',4'',5''-TRICHLOROACETANILIDE 98+%;Acetanilide, 2',4',5'-trichloro-
• CAS NO: 23627-24-9
• Molecular Formula: C₈H₆Cl₃NO
• Molecular Weight: 238.5
• EINECS: 245-793-6
• Mol File: 23627-24-9.mol
• Article Data: 5

Chemical Properties

• Melting Point: 186-188°C
• Boiling Point: 373.969 °C at 760 mmHg
• Flash Point: 179.97 °C
• Appearance: /
• Density: 1.506 g/cm³
• Vapor Pressure: 8.63E-06mmHg at 25°C
• Refractive Index: 1.614
• PKA: 12.65±0.70(Predicted)
• CAS DataBase Reference: 2,4,5-TRICHLOROACETANILIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,5-TRICHLOROACETANILIDE(23627-24-9)
• EPA Substance Registry System: 2,4,5-TRICHLOROACETANILIDE(23627-24-9)

Safety Data

• Safety Statements: 22-24/25
• RTECS: AE7890200
• Hazardous Substances Data: 23627-24-9(Hazardous Substances Data)

Usage

General Description

2,4,5-TRICHLOROACETANILIDE, also known as Tricamba, is a synthetic chemical compound used as a herbicide to control broadleaf weeds and brush in a variety of crops such as corn, wheat, and tobacco. It belongs to the chloroacetanilide chemical family, which is known for its selective weed-killing properties. Tricamba works by interfering with the growth processes of target plants, inhibiting their ability to produce essential proteins and ultimately leading to their death. It is typically applied as a liquid spray and is known for its effectiveness in controlling tough-to-kill weeds. However, there have been concerns about its potential risks to human health and the environment, leading to regulatory restrictions and controversy surrounding its use.

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

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

Downstream Products

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

Relevant articles and documents

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.

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.

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.