5469-05-6

Basic information

• Product Name: 1-(3,4-dimethoxyphenyl)but-3-en-1-yl acetate
• CAS NO: 5469-05-6
• Molecular Formula: C₁₄H₁₈O₄
• Molecular Weight: 250.2903
• Mol File: 5469-05-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 334.6°C at 760 mmHg
• Flash Point: 144.3°C
• Density: 1.062g/cm³
• Vapor Pressure: 0.000126mmHg at 25°C
• Refractive Index: 1.499
• CAS DataBase Reference: 1-(3,4-dimethoxyphenyl)but-3-en-1-yl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,4-dimethoxyphenyl)but-3-en-1-yl acetate(5469-05-6)
• EPA Substance Registry System: 1-(3,4-dimethoxyphenyl)but-3-en-1-yl acetate(5469-05-6)

Safety Data

• Hazardous Substances Data: 5469-05-6(Hazardous Substances Data)

Usage

Type of compound

Ester

Specific type

Acetate

Derived from

Combination of 1-(3,4-dimethoxyphenyl)but-3-en-1-ol and acetic acid

Common uses

Production of fragrances and flavors

Applications

Perfumes, soaps, and other scented products

Industry

Food industry as a flavoring agent

Pharmacological properties

Studied for potential properties

Precursor

Used as a precursor to other valuable chemical compounds

Upstream product

• 106-95-6 allyl bromide 
• 271771-50-7 1,1-diacetoxy-1-(3,4-dimethoxyphenyl)methane 
• 762-72-1 allyl-trimethyl-silane 
• 108-24-7 acetic anhydride 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 97387-80-9 1-(3,4-dimethoxy-phenyl)-but-3-en-1-ol 

Relevant articles and documents

Allylsamarium bromide-mediated cascade cyclization of homoallylic esters. Synthesis of 2-(2-hydroxyalkyl)cyclopropanols and 2-(2-hydroxyethyl)bicyclo[2.1.1]hexan-1-ols

In continuation of our previous study on the intramolecular reductive coupling of simple homoallylic esters promoted by allylSmBr/HMPA/H2O, which afforded a facile synthesis of 2-(2-hydroxyalkyl)cyclopropanols, here we report the reductive casc

LiBF4-Catalyzed three-component coupling of an aldehyde, acetic anhydride and allyltrimethylsilane/TMSCN

Lithium tetrafluoroborate is found to be an efficient catalyst for allylation and cyanation of aldehydes with allyltrimethylsilane and trimethylsilyl cyanide in the presence of acetic anhydride at room temperature to produce homoallylic acetates and α-cya

Scandium triflate catalyzed allylation of acetals and gem-diacetates: A facile synthesis of homoallyl ethers and acetates

Scandium triflate catalyzes efficiently the allylation reactions of acetals and gem-diacetates with allyltrimethylsilane at ambient temperature to afford the corresponding homoallyl ethers and acetates in high yields. Also it is found to be effective for