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54123-71-6

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54123-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54123-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,2 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54123-71:
(7*5)+(6*4)+(5*1)+(4*2)+(3*3)+(2*7)+(1*1)=96
96 % 10 = 6
So 54123-71-6 is a valid CAS Registry Number.

54123-71-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-2-methoxy-2-propen-1-one

1.2 Other means of identification

Product number -
Other names 2-Methoxy-1-phenyl-2-propen-1-on

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:54123-71-6 SDS

54123-71-6Relevant articles and documents

Iridium catalyst for catalyzing propargyl ester rearrangement to prepare substituted ketone compounds

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Paragraph 0057-0060, (2021/02/24)

The invention discloses an iridium catalyst for catalyzing propargyl ester rearrangement to prepare substituted ketone compounds, and belongs to the field of chemical materials. The iridium catalyst TriaIrX2 (wherein X is Cl, Br or I) is synthesized from (2H-1, 2, 3-triazole-1-yl) acetic acid as a ligand and iridium, and the iridium catalyst has excellent catalytic activity on a rearrangement reaction of propargyl ester compounds under mild conditions, has more efficient catalytic performance compared with a traditional catalyst, can improve the stereoselectivity of the reaction, and can improve the synthesis yield of the unsaturated substituted ketone compound. In addition, the catalyst can also be used for a reaction of preparing substituted ketone compounds from benzyl alcohol compoundsand acetophenone compounds and a synthesis reaction of bisphenol F, and the application prospect of the catalyst is wide.

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