1798-12-5

Basic information

• Product Name: [2-(acetylamino)phenoxy]acetic acid
• Synonyms: (2-Acetamidophenoxy)acetic acid; acetic acid, 2-[2-(acetylamino)phenoxy]-
• CAS NO: 1798-12-5
• Molecular Formula: C₁₀H₁₁NO₄
• Molecular Weight: 209.1986
• Mol File: 1798-12-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 426.1°C at 760 mmHg
• Flash Point: 211.5°C
• Density: 1.326g/cm³
• Vapor Pressure: 5.07E-08mmHg at 25°C
• Refractive Index: 1.592
• CAS DataBase Reference: [2-(acetylamino)phenoxy]acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: [2-(acetylamino)phenoxy]acetic acid(1798-12-5)
• EPA Substance Registry System: [2-(acetylamino)phenoxy]acetic acid(1798-12-5)

Safety Data

• Hazardous Substances Data: 1798-12-5(Hazardous Substances Data)

Usage

General Description

[2-(acetylamino)phenoxy]acetic acid is a synthetic organic compound known for its potential use as a herbicide. It belongs to the family of phenoxy herbicides and is used to control broadleaf weeds and woody plants. The chemical is derived from phenoxyacetic acid and has an acetylamino group attached to the phenyl ring. It works by mimicking the plant growth hormone auxin, causing the plant to grow uncontrollably and eventually leading to its death. [2-(acetylamino)phenoxy]acetic acid is of interest in agricultural and environmental applications, and its use is regulated in many regions due to potential environmental and health concerns.

Upstream product

• 79-11-8 chloroacetic acid 
• 614-80-2 2-(acetylamino)phenol 

Downstream Products

• 916656-23-0 dimethyl N-{[(2S)-2-({2-[2-(acetylamino)phenoxy]acetyl}amino)propyl]sulfonyl}-D-glutamate 
• 5466-88-6 3,4-dihydro-3-oxo-2H-1,4-benzoxazine 

Relevant articles and documents

Finding new elicitors that induce resistance in rice to the white-backed planthopper Sogatella furcifera

Herein we report a new way to identify chemical elicitors that induce resistance in rice to herbivores. Using this method, by quantifying the induction of chemicals for GUS activity in a specific screening system that we established previously, 5 candidate elicitors were selected from the 29 designed and synthesized phenoxyalkanoic acid derivatives. Bioassays confirmed that these candidate elicitors could induce plant defense and then repel feeding of white-backed planthopper Sogatella furcifera.

Potential anticancer agents--L. Non-classical antimetabolites. II. Some factors in the design of exoalkylating enzyme inhibitors, particulary of lactic dehydrogenase.

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