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3-Phenylpropenoic acid 2-methyl-2-propenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54889-46-2

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54889-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54889-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,8 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54889-46:
(7*5)+(6*4)+(5*8)+(4*8)+(3*9)+(2*4)+(1*6)=172
172 % 10 = 2
So 54889-46-2 is a valid CAS Registry Number.

54889-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylprop-2-enyl 3-phenylprop-2-enoate

1.2 Other means of identification

Product number -
Other names trans-cinnamic acid methallyl ester

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:54889-46-2 SDS

54889-46-2Relevant academic research and scientific papers

A 1,3,2-Diazaphospholene-Catalyzed Reductive Claisen Rearrangement

Reed, John H.,Donets, Pavel A.,Miaskiewicz, Solène,Cramer, Nicolai

supporting information, p. 8893 - 8897 (2019/05/28)

1,3,2-Diazaphospholenes (DAPs) are an emerging class of organic hydrides. In this work, we exploited them as efficient catalysts for very mild reductive Claisen rearrangements. The method is tolerant towards a wide variety of functional groups and operates at ambient temperature. Besides being enantiospecific for substrates with existing stereogenic centers, the diastereoselectivity can be switched by varying solvents and DAP catalysts. The reaction kinetics show direct rearrangements of O-bound phospholene enolates and provide a proof-of-principle for catalytic enantioselective reactions.

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