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1,4-Pentadien-3-one, 4-ethoxy-2-methyl-1-phenyl-, (1E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

647024-48-4

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647024-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 647024-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,7,0,2 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 647024-48:
(8*6)+(7*4)+(6*7)+(5*0)+(4*2)+(3*4)+(2*4)+(1*8)=154
154 % 10 = 4
So 647024-48-4 is a valid CAS Registry Number.

647024-48-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethoxy-2-methyl-1-phenylpenta-1,4-dien-3-one

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:647024-48-4 SDS

647024-48-4Relevant academic research and scientific papers

Enantioselective Nazarov Cyclizations Catalyzed by an Axial Chiral C6F5-Substituted Boron Lewis Acid

Süsse, Lars,Vogler, Maria,Mewald, Marius,Kemper, Benedict,Irran, Elisabeth,Oestreich, Martin

supporting information, p. 11441 - 11444 (2018/08/28)

A chiral variant of B(C6F5)3 with a 3,3′-disubstituted binaphthyl backbone is shown to catalyze Nazarov cyclizations with high levels of enantio- and diastereocontrol. The parent B(C6F5)3 a

The Palladium(II)-Catalyzed Nazarov Reaction

Bee, Cisco,Leclerc, Eric,Tius, Marcus A.

, p. 4927 - 4930 (2007/10/03)

(Equation presented) The PdCl2-catalyzed cyclization of α-alkoxy dienones leads to 2-hydroxycyclopentenones, whereas the Pd(OAc)2-catalyzed reaction leads to cross-conjugated cyclopentenones through an oxidative process.

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