40926-80-5

Basic information

• Product Name: (2,4,6-trichlorophenoxy)acetyl chloride
• CAS NO: 40926-80-5
• Molecular Formula: C₈H₄Cl₄O₂
• Molecular Weight: 273.9282
• Mol File: 40926-80-5.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 325.6°C at 760 mmHg
• Flash Point: 137.7°C
• Density: 1.571g/cm³
• Vapor Pressure: 0.000227mmHg at 25°C
• Refractive Index: 1.569
• CAS DataBase Reference: (2,4,6-trichlorophenoxy)acetyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: (2,4,6-trichlorophenoxy)acetyl chloride(40926-80-5)
• EPA Substance Registry System: (2,4,6-trichlorophenoxy)acetyl chloride(40926-80-5)

Safety Data

• Hazardous Substances Data: 40926-80-5(Hazardous Substances Data)

Usage

Description

(2,4,6-trichlorophenoxy)acetyl chloride is a chemical compound derived from acetyl chloride and phenoxyacetic acid, primarily utilized in the synthesis of herbicides and plant growth regulators. It is a toxic substance that requires careful handling to prevent health risks such as skin and eye irritation, respiratory, and digestive issues.

Uses

Used in Herbicide Production:
(2,4,6-trichlorophenoxy)acetyl chloride is used as a key intermediate in the synthesis of herbicides such as 2,4,5-T and 2,4-D for controlling weeds and unwanted vegetation in various agricultural and landscaping applications.
Used in Plant Growth Regulation:
In the agricultural industry, (2,4,6-trichlorophenoxy)acetyl chloride is used as a chemical component in the development of plant growth regulators, which help manage and control plant growth for optimal crop yield and quality.

Upstream product

• 575-89-3 2-(2,4,6-trichlorophenoxy)acetic acid 
• 88-06-2 2,4,6-Trichlorophenol 
• 3784-03-0 sodium 2,4,6-trichlorophenolate 

Downstream Products

• 14426-43-8 ethyl 2-(2,4,6-trichlorophenoxy)acetate 
• 626239-01-8 (2,4,6-trichloro-phenoxy)-acetic acid anilide 
• 855602-84-5 (2,4,6-trichloro-phenoxy)-ketene 
• 288611-50-7 (2,4,6-trichloro-phenoxy)-acetic acid amide 
• 92429-49-7 (2,4,6-trichloro-phenoxy)-acetic acid-(2,4,6-trichloro-phenoxymethyl ester) 
• 19443-45-9 N-(Octahydro-naphthalen-4a-yl)-2-(2,4,6-trichloro-phenoxy)-acetamide 
• 137537-07-6 1-Benzoimidazol-1-yl-2-(2,4,6-trichloro-phenoxy)-ethanone 
• 121989-66-0 N-Methoxy-2-(2,4,6-trichloro-phenoxy)-acetamide 
• 103436-00-6 N-ethyl-2,4,6-trichlorophenoxyacetamide 
• 15362-44-4 phenyl-(2,4,6-trichloro-phenyl)-amine 
• 63333-26-6 N-ethyl-2,4,6-trichloro-aniline 
• 626239-06-3 2-chloro-N-phenyl-N-(2,4,6-trichloro-phenyl)-acetamide 
• 626239-08-5 1-(2,4,6-trichloro-phenyl)-1,3-dihydro-indol-2-one 
• 101495-06-1 (2,4,6-trichloro-phenoxy)-acetonitrile 

Relevant articles and documents

Highly selective κ opioid analgesics. Synthesis and structure-activity relationships of novel N-[(2-aminocyclohexyl)aryl]acetamide and N-[(2-aminocyclohexyl)aryloxy]acetamide derivatives

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A convenient preparation of N-alkyl and N-arylamines by smiles rearrangement - Synthesis of analogues of diclofenac

Smiles rearrangement of substituted aryloxyacetamides in which oxygen and nitrogen are separated by COCH2 group has been successful even when the aryloxy ring carries weak or no electron withdrawing group. Earlier reports of such reactions involved either strong electron withdrawing groups or a special catalyst. The diphenylamines thus obtained gave analogues of diclofenac in only one case.

Biological Evaluation of some New Nitrophenoxy/Halophenoxyaeetyl/Propionyl-2-mercaptobenzothiazoles

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