1002502-24-0

Basic information

• Product Name: 2-(2,6-dichlorophenoxy)-N-p-tolylacetaMide
• Synonyms: 2-(2,6-dichlorophenoxy)-N-p-tolylacetaMide
• CAS NO: 1002502-24-0
• Molecular Formula: C₁₅H₁₃Cl₂NO₂
• Molecular Weight: 310.17522
• Mol File: 1002502-24-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2,6-dichlorophenoxy)-N-p-tolylacetaMide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,6-dichlorophenoxy)-N-p-tolylacetaMide(1002502-24-0)
• EPA Substance Registry System: 2-(2,6-dichlorophenoxy)-N-p-tolylacetaMide(1002502-24-0)

Safety Data

• Hazardous Substances Data: 1002502-24-0(Hazardous Substances Data)

Usage

Common uses

Herbicide and plant growth regulator It is widely used in agriculture to control weeds and regulate the growth of plants.

Mode of action

Disrupting the growth of unwanted plants The compound works by interfering with the normal growth processes of target plants, making it an effective tool for weed control.

Physical properties

White crystalline solid This describes the appearance and texture of the compound.

Solubility

Slightly soluble in water The compound does not dissolve easily in water, which may affect its application and behavior in the environment.

Melting point

151-153°C The temperature range at which the compound transitions from a solid to a liquid state.

Persistence

Long half-life in the soil The compound remains active in the soil for an extended period, contributing to its effectiveness as a herbicide.

Safety precautions

Harmful if inhaled or ingested The compound can pose health risks if it enters the body through breathing or ingestion.

Potential irritation

May cause skin and eye irritation The compound can cause discomfort or damage to the skin and eyes upon contact, emphasizing the need for proper handling and protective measures.

Upstream product

• 87-65-0 2,6-Dichlorophenol 
• 16634-82-5 N-(p-tolyl)-2-chloroacetamide 

Downstream Products

• 332903-75-0 2-chloro-N-(2',6'-dichloro-phenyl)-N-p-tolyl-acetamide 
• 332903-73-8 N-(2',6'-Dichlorophenyl)-4-methylaniline 

Relevant articles and documents

Synthesis of new N-aryl oxindoles as intermediates for pharmacologically active compounds

Various new N-aryl oxindoles were synthesized as intermediates for the preparation of pharmacologically active 2-(N-arylamino)-phenylacetic acids. Two novel approaches were explored for the construction of diarylamine and N-aryl oxindole core structures, in addition to Buchwald-arylamination and Smiles rearrangement. Condensation of anilines with 2-oxo-cyclohexylidene-acetic acid derivatives and subsequent dehydrogenation is a new and viable method for the preparation of N-aryl oxindoles. Graphical Abstract.