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1-(-Ethoxyethoxy)-1,2-propadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20524-89-4

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20524-89-4 Usage

Physical state

Colorless liquid

Odor

Slightly sweet

Usage

a. Solvent
b. Monomer in polymerization reactions
c. Production of resins
d. Production of coatings
e. Production of adhesives

Toxicity

Low toxicity

Environmental impact

Not known to be harmful to the environment

Safety precautions

Proper handling and storage required to prevent potential hazards

Check Digit Verification of cas no

The CAS Registry Mumber 20524-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,2 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20524-89:
(7*2)+(6*0)+(5*5)+(4*2)+(3*4)+(2*8)+(1*9)=84
84 % 10 = 4
So 20524-89-4 is a valid CAS Registry Number.

20524-89-4SDS

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-(1-ethoxyethoxy)propa-1,2-diene

1.2 Other means of identification

Product number -
Other names 1-ethoxyethoxyallene

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:20524-89-4 SDS

20524-89-4Relevant academic research and scientific papers

One-Pot Synthesis of 1-(1-Alkoxyethoxy)allenes

Tarasova,Nedolya,Albanov

, p. 1831 - 1834 (2019/03/26)

A convenient one-pot procedure has been proposed for the preparation of 1-(1-alkoxyethoxy)allenes from alkoxyethenes and prop-2-yn-1-ol with the use of trifluoroacetic acid as highly efficient catalyst for the synthesis of 3-(1-alkoxyethoxy)prop-1-ynes and of the system t-BuOK–DMSO for the isomerization of the latter into allenes.

Synthesis of 3-hydroxy-1-methyl-2-(methylthio)pyrrole from methyl isothiocyanate and prop-2-yn-1-ol

Brandsma,Nedolya,Trofimov

, p. 1634 - 1636 (2007/10/03)

A methylated adduct of lithiated 1-(1-ethoxyethoxy)allene and methyl isothiocyanate undergoes intramolecular cyclization in the presence of CuBr to give 3-(1-ethoxyethoxy)-1-methyl-2-(methylthio)pyrrole. The methanolysis of the latter affords 3-hydroxy-1-methyl-2-(methylthio)pyrrole.

ALLENE ETHERS FOR THE CATIONIC CYCLOPENTANNELATION

Tius, Marcus A.,Ousset, J-B.,Astrab, Donald P.,Fauq, Abdul H.,Trehan, Sanjay

, p. 923 - 924 (2007/10/02)

Only allene ethers having a group which is capable of departing as a stable cation participate successfully in the cationic cyclopentannelation reaction.

SILYL KETONE CHEMISTRY. PREPARATION AND REACTIONS OF UNSATURATED SILYL KETONES

Reich, Hans J.,Kelly, Martha J.,Olson, Richard E.,Holtan, Ronald C.

, p. 949 - 960 (2007/10/02)

A series of silyl ketones has been prepared by appropriate manipulation of α-silylated allenol ethers.Among the compounds prepared were alkenyl, alkynyl and acyl silyl ketones.The spectroscopic properties of representative members of these classes of comp

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