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Ethanone, 1-(2-ethyl-4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41068-29-5

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41068-29-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41068-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,6 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41068-29:
(7*4)+(6*1)+(5*0)+(4*6)+(3*8)+(2*2)+(1*9)=95
95 % 10 = 5
So 41068-29-5 is a valid CAS Registry Number.

41068-29-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-ethyl-4-methoxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 4-Methoxy-2-ethyl-acetophenon

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:41068-29-5 SDS

41068-29-5Relevant academic research and scientific papers

BICYCLIC COMPOUND AND USE THEREOF FOR INHIBITING SUV39H2

-

, (2017/08/01)

The present invention directs to a compound represented by formula (I).

Ruthenium-catalysed ortho alkylation of hydroxyacetophenones; the functionalisation of ring C aromatic diterpenoids

Harris, Paul W.R.,Woodgate, Paul D.

, p. 211 - 223 (2007/10/03)

Ortho C-H bond coupling of some 2-alkoxyacetophenones with olefins catalysed by ruthenium complexes results in a high yield of the ortho alkylated product, providing that a suitable protecting group is employed. No such protection was required for a para-alkoxy group; an activating effect was also observed. Bicyclic and tricyclic analogues react similarly.

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