2088-24-6

Basic information

• Product Name: 3-METHOXYPHENOXYACETIC ACID
• Synonyms: ASISCHEM B51646;AURORA 22719;IFLAB-BB F1924-0025;LABOTEST-BB LT00454267;3-METHOXYPHENOXYACETIC ACID;AKOS BBS-00007934;AKOS BC-1582;(M-METHOXYPHENOXY)ACETIC ACID
• CAS NO: 2088-24-6
• Molecular Formula: C₉H₁₀O₄
• Molecular Weight: 182.17
• Product Categories: Phenoxyacetic Acids and Alcohols (substituted)
• Mol File: 2088-24-6.mol
• Article Data: 19

Chemical Properties

• Melting Point: 116-117°C
• Boiling Point: 325.9°Cat760mmHg
• Flash Point: 131.9°C
• Appearance: /
• Density: 1.226g/cm³
• Vapor Pressure: 9.11E-05mmHg at 25°C
• Refractive Index: 1.528
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: pK1:3.141 (25°C)
• BRN: 1876898
• CAS DataBase Reference: 3-METHOXYPHENOXYACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-METHOXYPHENOXYACETIC ACID(2088-24-6)
• EPA Substance Registry System: 3-METHOXYPHENOXYACETIC ACID(2088-24-6)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 36/37/38-22
• Safety Statements: 26-36
• HazardClass: IRRITANT
• Hazardous Substances Data: 2088-24-6(Hazardous Substances Data)

Usage

General Description

3-Methoxyphenoxyacetic acid is a chemical compound with the molecular formula C9H10O4. It is a synthetic auxin, a type of plant growth regulator that stimulates cell elongation and division, and is commonly used in agriculture to control the growth and development of plants. 3-Methoxyphenoxyacetic acid is primarily used as a herbicide, acting as a post-emergent selective herbicide for the control of broadleaf weeds in various crops, including cereals, corn, and sugarcane. It works by disrupting the growth and development of weeds, leading to their eventual death. Additionally, it has been studied for its potential use in tissue culture and as a growth promoter for plants. 3-Methoxyphenoxyacetic acid is a white crystalline solid with a slight odor and is considered to be moderately toxic, with potential adverse effects on human health and the environment.

InChI:InChI=1/C9H10O4/c1-12-7-3-2-4-8(5-7)13-6-9(10)11/h2-5H,6H2,1H3,(H,10,11)

Upstream product

• 82815-86-9 (3-methoxy-phenoxy)-acetic acid ethyl ester 
• 52116-39-9 2-carboxymethoxy-4-methoxy-benzoic acid 
• 1122-95-8 sodium 4-methoxyphenolate 
• 3926-62-3 sodium monochloroacetic acid 
• 150-19-6 O-methylresorcine 
• 79-11-8 chloroacetic acid 
• 105-36-2 ethyl bromoacetate 
• 81720-20-9 methyl (3-methoxyphenoxy)acetate 
• 7732-18-5 water 
• 79-14-1 glycolic Acid 
• 766-85-8 3-methoxy-1-iodobenzene 

Downstream Products

• 82815-86-9 (3-methoxy-phenoxy)-acetic acid ethyl ester 
• 500891-55-4 6-methoxy-benzofuran-3-ol 
• 106967-74-2 2-(3-methoxyphenoxy)acetyl chloride 
• 198905-40-7 2-(3-methoxyphenoxy)acetamide 
• 860743-61-9 (5-methoxy-2,4-dinitro-phenoxy)-acetic acid 
• 1836-25-5 3-Hydroxy-4-butyryl-phenoxyessigsaeure 
• 81720-20-9 methyl (3-methoxyphenoxy)acetate 
• 15832-09-4 6-methoxy-3-coumaranone 
• 150-19-6 O-methylresorcine 
• 124-38-9 carbon dioxide 
• 201230-82-2 carbon monoxide 
• 74767-54-7 2-benzoyloxy-6-methoxycoumaran-3-one 
• 436155-36-1 2-(3-methoxyphenoxy)acetylhydrazine 
• 71706-76-8 1-(3-methoxy-phenoxy)-3-phenyl-acetone 

Relevant articles and documents

Design and Synthesis of New 1,3,4-Oxadiazole - Benzothiazole and Hydrazone Derivatives as Promising Chemotherapeutic Agents

Looking for new cytotoxic and antimicrobial agents with improved antitumor activity, a series of hydrazide and oxadiazole derivatives were designed and synthesized using 3-methoxyphenol as starting substance. Novel N'-(arylidene)-2-(3-methoxyphenoxy)aceto

PRMT5 INHIBITORS AND USES THEREOF

Described herein are compounds of Formula (I), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting PRMT5 activity. Methods of using the compounds for treating PRMT5-mediated disorders are also described.

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.