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diethyl 4-benzoyl-1-oxo-1-phenylpent-4-en-2-yl phosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1217357-17-9

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1217357-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1217357-17-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,3,5 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1217357-17:
(9*1)+(8*2)+(7*1)+(6*7)+(5*3)+(4*5)+(3*7)+(2*1)+(1*7)=139
139 % 10 = 9
So 1217357-17-9 is a valid CAS Registry Number.

1217357-17-9SDS

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 diethyl 4-benzoyl-1-oxo-1-phenylpent-4-en-2-yl phosphonate

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:1217357-17-9 SDS

1217357-17-9Relevant academic research and scientific papers

A Synthetic and Computational Investigation into the Direct Synthesis of α -Hydroxymethylated Enones from β-keto Phosphonates

Ryan, Sarah J.,Thompson, Christopher D.,Lupton, David W.

experimental part, p. 720 - 727 (2010/02/16)

The synthesis of a range of -hydroxymethylated enones has been achieved using the Villiras modification of the HornerWadsworthEmmons (HWE) reaction. Scope, limitations, and mechanistic aspects of this reaction were investigated using a combination of synthetic and computational studies. These investigations support a SchlosserCorey type reaction mechanism that is balanced between two pathways with the outcome influenced by the steric environment of the substrate. CSIRO 2009.

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