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2-Butanone, 4-(2,4,6-trimethoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53581-92-3

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53581-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53581-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,8 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53581-92:
(7*5)+(6*3)+(5*5)+(4*8)+(3*1)+(2*9)+(1*2)=133
133 % 10 = 3
So 53581-92-3 is a valid CAS Registry Number.

53581-92-3SDS

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-(2,4,6-trimethoxyphenyl)butan-2-one

1.2 Other means of identification

Product number -
Other names 2-Butanone,4-(2,4,6-trimethoxyphenyl)

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:53581-92-3 SDS

53581-92-3Downstream Products

53581-92-3Relevant academic research and scientific papers

A rapid and highly efficient Michael addition of methoxybenzenes and indoles to α,β-unsaturated ketones using BF3·OEt2 as a catalyst

Swetha,Raghavender Reddy,Madhu Babu,Meshram

supporting information, p. 4427 - 4431 (2017/10/30)

An efficient and general protocol is described for the Michael addition of α,β-unsaturated ketones with electron-rich arenes/indoles to give alkylated arenes/indoles under mild reaction condition at room temperature. Shorter reaction time, convenient and

Heterobimetallic Pd-Sn catalysis: Michael addition reaction with C-, N-, O-, and S-nucleophiles and in situ diagnostics

Das, Debjit,Pratihar, Sanjay,Roy, Sujit

supporting information, p. 2430 - 2442 (2013/04/23)

An efficient Michael addition reaction of differently substituted enones with carbon, sulfur, oxygen, and nitrogen nucleophiles has been achieved by a new heterobimetallic "Pd-Sn" catalyst system. The nature of the catalytically relevant species and their

Addition of heterocycles to electron deficient olefins and alkynes catalyzed by gold(III)

Li, Zigang,Shi, Zhangjie,He, Chuan

, p. 5049 - 5054 (2007/10/03)

A gold(III)-catalyzed hydroarylation of different olefins is reported here. AuCl3 works as an excellent catalyst to mediate reactions between various heterocycles and electron deficient olefins and alkynes under mild conditions. This gold(III)-based method tolerates different functional groups such as aldehyde, carboxylic acid, nitrile, and is highly efficient. We have shown that some of these reactions complete in minutes at room temperature.

Gold(III) Chloride-Catalyzed Addition Reactions of Electron-Rich Arenes to Methyl Vinyl Ketone

Dyker, Gerald,Muth, Enrico,Hashmi, A. Stephen K.,Ding, Li

, p. 1247 - 1252 (2007/10/03)

For the reaction of α,β-unsaturated ketones with electron-rich arenes catalyzed by gold(III) chloride both, a Friedel-Crafts-type mechanism and an initial metallation, are evaluated. Gold(III) chloride has proven to be an efficient catalyst under very mod

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