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2-(3,4-dimethoxyphenyl)ethyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14617-41-5

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14617-41-5 Usage

Compound type

Ester

Constituents

Acetate group and 2-(3,4-dimethoxyphenyl)ethyl group

Usage

Fragrance and flavor industry

Aroma

Sweet, floral

Applications

Perfumes, flavoring agent in food and beverages, potential use in pharmaceuticals and cosmetics

Value

Pleasant odor and flavor, valuable ingredient in consumer products

Check Digit Verification of cas no

The CAS Registry Mumber 14617-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,1 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14617-41:
(7*1)+(6*4)+(5*6)+(4*1)+(3*7)+(2*4)+(1*1)=95
95 % 10 = 5
So 14617-41-5 is a valid CAS Registry Number.

14617-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-dimethoxyphenyl)ethyl acetate

1.2 Other means of identification

Product number -
Other names Benzeneethanol,-3,4-dimethoxy,acetate

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:14617-41-5 SDS

14617-41-5Relevant academic research and scientific papers

Binap-silver salts as chiral catalysts for the enantioselective 1,3-dipolar cycloaddition of azomethine ylides and alkenes

Mancebo-Aracil, Juan,Martin-Rodriguez, Maria,Najera, Carmen,Sansano, Jose M.,Costa, Paulo R.R.,De Lima, Evanoel Crizanto,Dias, Ayres G.

, p. 1596 - 1606 (2013/02/23)

Binap-AgSbF6 catalyzed 1,3-dipolar cycloadditions between azomethine ylides and electrophilic alkenes are described and compared with analogous transformations mediated by other Binap-silver(I) salt complexes. Maleimides and 1,2-bis(phenylsulfo

Dichloromethylenation of Lactones. 6. Efficient Synthesis of Dichloroolefins from Lactones and Acetates Using Triphenylphosphine and Tetrachloromethane

Lakhrissi, Mohamed,Chapleur, Yves

, p. 5752 - 5757 (2007/10/02)

Triphenylphosphine and tetrachloromethane react cleanly in refluxing tetrahydrofuran with substituted γ- and δ-lactones and some esters to afford the corresponding dichloroolefins in good yields.This new Wittig-type reaction provides an easy entry to this new class of compounds and tolerates a large of protecting groups.Application of this methodology to the dichloroolefination of simple lactones, suger-derived lactones, and other biologically significant lactones is described.

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