17598-03-7

Basic information

• Product Name: 2,4,5-trimethoxystyrene
• Synonyms: 2,4,5-trimethoxystyrene
• CAS NO: 17598-03-7
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 0
• Mol File: 17598-03-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 302.2°C at 760 mmHg
• Flash Point: 100.7°C
• Appearance: /
• Density: 1.036g/cm³
• Vapor Pressure: 0.0018mmHg at 25°C
• Refractive Index: 1.522
• CAS DataBase Reference: 2,4,5-trimethoxystyrene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,5-trimethoxystyrene(17598-03-7)
• EPA Substance Registry System: 2,4,5-trimethoxystyrene(17598-03-7)

Safety Data

• Hazardous Substances Data: 17598-03-7(Hazardous Substances Data)

Usage

Class

methoxyphenols

Appearance

colorless to pale yellow liquid

Odor

sweet, floral

Uses

flavoring agent in food industry, fragrance ingredient in perfumery industry

Potential applications

organic synthesis, material science

Medicinal properties

anticancer, anti-inflammatory activities

InChI:InChI=1/C11H14O3/c1-5-8-6-10(13-3)11(14-4)7-9(8)12-2/h5-7H,1H2,2-4H3

Upstream product

• 4460-86-0 asaraldehyde 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 135-77-3 1,2,4-trimethoxy-benzene 
• 41317-93-5 2,4,5-trimethoxy-α-methylbenzenemethanol 
• 1818-28-6 2',4',5'-trimethoxyacetophenone 

Downstream Products

• 4460-86-0 asaraldehyde 
• 1646623-55-3 2-(methylsulfonyl)-1-(2,4,5-trimethoxyphenyl)ethanone 
• 1306770-73-9 C₂₂H₂₈O₆ 

Relevant articles and documents

COMPOUNDS AND THE USE THEREOF IN METATHESIS REACTIONS

The disclosure provides Group 6 complexes, which, in some embodiments, are useful for catalyzing olefin metathesis reactions. In some embodiments, the compounds are compounds of the following formula (I) wherein: M is a Group 6 metal atom; X is an oxygen

Synthesis and hypolipidemic activity of modified side chain α-asarone homologues

A series of homologues of α-asarone (1), containing variable size and functionality on the side chain attached to the aromatic ring, has been subjected to a study of structure-activity relationship. For most of the prepared derivatives, either with a carbonyl (8a-8e), a hydroxy group (9a-9e), or with a conjugated double bond (10a-10d), significant effects on serum lipoprotein cholesterol, LDL-cholesterol, HDL-cholesterol and triglycerides were displayed. The results showed an enhancement of the hypocholesterolemic activity as the length of the chain is decreased. Theoretical conformational and electrostatic potential analyses of 1 and olefins 10 suggest unfavorable steric interactions in the bulky superior side-chain homologues as the deactivating biological effect.