95459-73-7

Basic information

• Product Name: 2-(3,4-DiMethoxyphenoxy)acetic Acid
• Synonyms: 2-(3,4-DiMethoxyphenoxy)acetic Acid
• CAS NO: 95459-73-7
• Molecular Formula: C₁₀H₁₂O₅
• Molecular Weight: 212.19928
• Product Categories: Aromatics, Intermediates, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 95459-73-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 354.9°C at 760 mmHg
• Flash Point: 139.4°C
• Appearance: /
• Density: 1.229g/cm³
• Vapor Pressure: 1.19E-05mmHg at 25°C
• Refractive Index: 1.52
• CAS DataBase Reference: 2-(3,4-DiMethoxyphenoxy)acetic Acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,4-DiMethoxyphenoxy)acetic Acid(95459-73-7)
• EPA Substance Registry System: 2-(3,4-DiMethoxyphenoxy)acetic Acid(95459-73-7)

Safety Data

• Hazardous Substances Data: 95459-73-7(Hazardous Substances Data)

Usage

Description

2-(3,4-DiMethoxyphenoxy)acetic Acid is an organic compound that serves as an intermediate in the synthesis of Rotenone, a naturally occurring broad-spectrum insecticide found in the seeds and stems of various plants.

Uses

Used in Pesticide Industry:
2-(3,4-DiMethoxyphenoxy)acetic Acid is used as a chemical intermediate for the production of Rotenone (R700580), a broad-spectrum insecticide. Rotenone is effective against a wide range of insects and is derived from natural sources, making it a preferred choice for environmentally friendly pest control solutions.

InChI:InChI=1/C10H12O5/c1-13-8-4-3-7(5-9(8)14-2)15-6-10(11)12/h3-5H,6H2,1-2H3,(H,11,12)

Upstream product

• 2033-89-8 3,4-dimethoxyphenol 
• 105-36-2 ethyl bromoacetate 
• 3926-62-3 sodium monochloroacetic acid 
• 623-48-3 ethyl iodoacetae 
• 105-39-5 chloroacetic acid ethyl ester 
• 41630-76-6 3,4-Dimethoxyphenoxyessigsaeureethylester 
• 530-81-4 2-carboxymethoxy-4,5-dimethoxy-benzoic acid 

Downstream Products

• 436155-39-4 methyl 2-(3,4-dimethoxyphenoxy)acetate 
• 859946-33-1 (4,5-dimethoxy-2-nitro-phenoxy)-acetic acid 
• 685144-65-4 (Z)-2-(3,4-Dimethoxy-phenoxy)-3-dimethylamino-acrylic acid methyl ester 
• 117364-96-2 3,4-dimethoxyphenoxyacetic chloride 
• 1610767-17-3 C₂₄H₂₉N₃O₆ 
• 3341-36-4 N-(3,4-dimethoxyphenylethyl)-2-phenoxyacetamide 

Relevant articles and documents

Benzoic acid derivative as well as preparation method and medicinal application thereof

The invention discloses a benzoic acid derivative as well as a preparation method and a pharmaceutical application thereof, and belongs to the technical field of medicines. The invention specifically discloses a benzoic acid derivative represented by a co

An efficient synthesis of benzofurans and their application in the preparation of natural products of the genus Calea

The intramolecular cyclization of the β-substituted olefins methyl 2-aryloxy-3-dimethylaminopropenoates 3a-3f catalyzed by Lewis acids leads to a short and novel synthesis of benzofurans 2a-2f. When the olefins 4-dimethylamino-3-aryloxy-3-buten-2-ones 4a-4f were used, the cyclization process was faster and provided the corresponding substituted 2-acetylbenzofurans 1a-1f. Among the latter, naturally occurring compounds calebertin (1a), caleprunin A (1b), and caleprunin B (1c) were prepared in good overall yields. These benzofurans were also obtained by direct treatment under MW irradiation of the precursors 1-aryloxypropan-2-ones 7a-7c with DMFDMA, followed by addition of the catalyst, resulting in a route that was one step shorter.

Phenylacetamide derivatives

A phenylacetamide derivative of formula (I) have potent analgesic and anti-inflammatory activities and exhibit less irritability and toxicity: STR1 wherein, X, Y, W, n, m and Ar are as defined in the specification.