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5658-50-4

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5658-50-4 Usage

Preparation

Obtained by reaction of 5% ethanolic potassium hydroxide with 2-(3,4,5-trimethoxybenzoyl)-2-methylacetic acid ethyl ester (m.p. 40°) at 60° for 1 h(76%).

Check Digit Verification of cas no

The CAS Registry Mumber 5658-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5658-50:
(6*5)+(5*6)+(4*5)+(3*8)+(2*5)+(1*0)=114
114 % 10 = 4
So 5658-50-4 is a valid CAS Registry Number.

5658-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,4,5-trimethoxyphenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names Propiophenone,3',4',5'-trimethoxy

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:5658-50-4 SDS

5658-50-4Relevant articles and documents

Alpha,beta-unsaturated ketone derivatives, preparation method of derivatives and application of derivatives as medicines

-

Paragraph 0073-0074; 0077-0078, (2019/12/15)

The invention relates to the technical field of medicine, and proposes alpha,beta-unsaturated ketone derivatives and a preparation method thereof. The derivatives have a structural general formula represented by a formula I shown in the specification, whe

Magnesium salt promoted tandem nucleophilic addition-Oppenauer oxidation of aldehydes with organozinc reagents

Fu, Ying,Zhao, Xing Ling,Hügel, Hulmet,Huang, Danfeng,Du, Zhengyin,Wang, Kehu,Hu, Yulai

supporting information, p. 9720 - 9724 (2016/10/31)

A magnesium salt promoted synthesis of ketones via tandem nucleophilic addition-Oppenauer oxidation of aldehydes using organozinc chemistry was demonstrated. Magnesium salts concomitantly generated via magnesium metal mediated organohalide zincation exhibit high efficacy for nucleophilic addition of organozinc reagents to aromatic aldehydes and thereafter Oppenauer oxidation whereby ketones are formed in high to excellent yields.

Efficient synthesis of alkyl aryl ketones & ketals via palladium-catalyzed regioselective arylation of vinyl ethers

Liu, Mingcui,Hyder, Zeynab,Sun, Yawei,Tang, Weijun,Xu, Lijin,Xiao, Jianliang

supporting information; experimental part, p. 2012 - 2015 (2010/07/04)

The combination of Pd(OAc)2 with 1,3-bis(diphenylphosphino) propane (dppp) in ethylene glycol constitutes a high-performance catalytic system for highly regioselective arylation of a range of electron-rich vinyl ethers by aryl bromides to provide, upon hydrolysis, alkyl aryl ketones and cyclic ketals in good yields with up to 3.75 × 105 TON and 15625 h-1 TOF.

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