Welcome to LookChem.com Sign In|Join Free
  • or
1-(3,4-dimethoxyphenyl)but-3-en-1-yl acetate is a chemical compound with the molecular formula C13H16O4. It is an organic ester derived from the parent compound but-3-en-1-yl acetate, with a 3,4-dimethoxyphenyl group attached to the butenyl chain. 1-(3,4-dimethoxyphenyl)but-3-en-1-yl acetate is characterized by its aromatic and fruity odor, and it is commonly used as a fragrance ingredient in various applications, such as perfumes, cosmetics, and personal care products. The presence of the dimethoxyphenyl group contributes to its unique scent profile, making it a valuable component in the creation of complex and pleasant aromas.

5469-05-6

Post Buying Request

5469-05-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5469-05-6 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

Check Digit Verification of cas no

The CAS Registry Mumber 5469-05-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5469-05:
(6*5)+(5*4)+(4*6)+(3*9)+(2*0)+(1*5)=106
106 % 10 = 6
So 5469-05-6 is a valid CAS Registry Number.

5469-05-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,4-dimethoxyphenyl)but-3-enyl acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5469-05-6 SDS

5469-05-6Downstream Products

5469-05-6Relevant academic research and scientific papers

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

Shen, Mengmeng,Tu, Yawei,Xie, Guanqun,Niu, Qingsheng,Mao, Hui,Xie, Tingting,Flowers, Robert A.,Lv, Xin,Wang, Xiaoxia

, p. 52 - 61 (2016/09/12)

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

Study on the coupling of acyclic esters with alkenes - The synthesis of 2-(2-hydroxyalkyl)cyclopropanols via cascade cyclization using allylsamarium bromide

Tu, Yawei,Zhou, Liejin,Yin, Ruifeng,Lv, Xin,Flowers Ii, Robert A.,Choquette, Kimberly A.,Liu, Huili,Niu, Qingsheng,Wang, Xiaoxia

, p. 11026 - 11028 (2013/01/15)

The radical cyclization between aliphatic acyclic esters and alkenes was achieved unprecedentedly in the presence of allylsamarium bromide with HMPA and H2O as additives. The cascade radical cyclization-ring-opening- anionic cyclization allowed facile and efficient access to 2-(2-hydroxyalkyl) cyclopropanols from readily available materials.

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

Yadav,Reddy, B.V. Subba,Vishnumurthy,Chary, Ch. Janardhana

, p. 5915 - 5918 (2008/02/10)

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

Indium(III) chloride catalyzed allylation of gem-diacetates: A facile synthesis of homoallyl acetates

Yadav,Subba Reddy,Madhuri,Sabitha

, p. 18 - 19 (2007/10/03)

Indium(III) chloride is found to catalyze efficiently the allylation of gem-diacetates with allyltrimethylsilane at room temperature to afford the corresponding homoallylic acetates in high yields with good regioselectivity.

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

Yadav, Jhillu S.,Subba Reddy, Basi V.,Srihari

, p. 673 - 675 (2007/10/03)

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

Indium-mediated allylation of gem-diacetates to homoallylic acetates in aqueous media

Yadav,Subba Reddy,Kiran Kumar Reddy

, p. 2695 - 2697 (2007/10/03)

Indium-mediated allylation of gem-diacetates gave excellent yields of the corresponding homoallylic acetates in aqueous media. (C) 2000 Elsevier Science Ltd.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 5469-05-6