67827-55-8

Basic information

• Product Name: 1,3,5-Trimethoxy-2-ethylbenzene
• Synonyms: 1,3,5-Trimethoxy-2-ethylbenzene;1-Ethyl-2,4,6-trimethoxybenzene;2-Ethyl-1,3,5-trimethoxybenzene
• CAS NO: 67827-55-8
• Molecular Formula: C₁₁H₁₆O₃
• Molecular Weight: 196.2429
• Mol File: 67827-55-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 275.9°Cat760mmHg
• Flash Point: 91.2°C
• Appearance: /
• Density: 1.01g/cm³
• Vapor Pressure: 0.00835mmHg at 25°C
• Refractive Index: 1.486
• CAS DataBase Reference: 1,3,5-Trimethoxy-2-ethylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Trimethoxy-2-ethylbenzene(67827-55-8)
• EPA Substance Registry System: 1,3,5-Trimethoxy-2-ethylbenzene(67827-55-8)

Safety Data

• Hazardous Substances Data: 67827-55-8(Hazardous Substances Data)

Usage

Physical state

Colorless to pale yellow liquid

Usage

Primarily used as a fragrance ingredient

Chemical class

Methoxyphenols (compounds containing a methoxy group attached to the benzene ring of a phenol moiety)

Additional uses

Commonly used as a flavoring agent

Presence

Often found in perfumes and other cosmetic products

Odor

Sweet, floral

Safety

Considered safe for use in applications when used in accordance with good manufacturing or feeding practice

InChI:InChI=1/C11H16O3/c1-5-9-10(13-3)6-8(12-2)7-11(9)14-4/h6-7H,5H2,1-4H3

Upstream product

• 621-23-8 1,2,3-trimethoxybenzene 
• 141-78-6 ethyl acetate 
• 832-87-1 2-(2,4,6-trimethoxyphenyl)ethan-1-ol 
• 106800-22-0 2-(2,4,6-trimethoxyphenyl)ethyl bromide 
• 13211-15-9 (+-)-camphenilone 
• 832-58-6 1-(2,4,6-trimethoxyphenyl)ethanone 
• 408310-30-5 2,2,2-trichloro-1-(2,4,6-trimethoxy-phenyl)-ethanone 

Downstream Products

• 19672-01-6 2-ethyl-3,5-dimethoxyphenol 
• 106800-34-4 4-ethyl-3,5-dimethoxy-phenol 
• 861531-73-9 3-ethyl-2,4,6,3',4'-pentamethoxy-benzophenone 

Relevant articles and documents

Hydrosilanes are not always a reducing reagent: A ruthenium-catalyzed introduction of primary alkyl groups to electron-rich aromatic rings using esters as a source of the alkyl groups

A triruthenium cluster, (μ3, η2, η3, η5-acenaphthylene)Ru3(CO) 7 effectively catalyzes primary-alkylation reaction of electron-rich aromatic rings using a combination of hydrosilane and est

Hydroxyl-Directed Regioselective Monodemethylation of Polymethoxyarenes

Methoxyl groups ortho to β-hydroxyethyl or γ-hydroxypropyl substituents in polymethoxybenzene derivatives were regioselectively demethylated with sodium thioethoxide in N,N-dimethylformamide.Methoxydihydrobenzofurans or methoxychromans were produced by cyclization of the monodemethylated β-hydroxyethyl or γ-hydroxypropyl derivatives, respectively.