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1-Propanone, 1-(3,4-dimethoxyphenyl)-2-[(4-methylphenyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

169210-71-3

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169210-71-3 Usage

Molecular structure

A complex organic compound with a propanone backbone, a 3,4-dimethoxyphenyl group, and a 4-methylphenylthio group as substituents.

Usage

Commonly used in organic synthesis, particularly for the production of pharmaceuticals and other fine chemicals.

Applications

Potential applications in the field of materials science, as a reagent or intermediate in chemical reactions.

Property variability

Specific properties and uses may vary depending on the context in which the compound is employed.

Check Digit Verification of cas no

The CAS Registry Mumber 169210-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,2,1 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 169210-71:
(8*1)+(7*6)+(6*9)+(5*2)+(4*1)+(3*0)+(2*7)+(1*1)=133
133 % 10 = 3
So 169210-71-3 is a valid CAS Registry Number.

169210-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,4-dimethoxyphenyl)-2-(4-methylphenyl)sulfanylpropan-1-one

1.2 Other means of identification

Product number -
Other names 3,4-dimethoxy-8-(4'-methylthiophenoxy)propiophenone

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:169210-71-3 SDS

169210-71-3Downstream Products

169210-71-3Relevant academic research and scientific papers

Structure-activity relationship of antileishmanials neolignan analogues

Aveniente, Mario,Pinto, Eduardo F.,Santos, Lourivaldo S.,Rossi-Bergmann, Bartira,Barata, Lauro E.S.

, p. 7337 - 7343 (2007)

Twenty-two synthetic analogues of neolignans comprising β-ketoethers and β-ketosulfides were obtained from condensation reactions among β-bromoketones and phenols or thiophenols, respectively, in basic solutions, and assayed in vitro for activity against

Anti-leishmanial activity of neolignans from Virola species and synthetic analogues

Barata, Lauro E.S,Santos, Lourivaldo S,Ferri, Pedro H,Phillipson, J.David,Paine, Angela,Croft, Simon L

, p. 589 - 595 (2007/10/03)

Surinamensin, a neolignan isolated from Virola surinamensis, 3,4,5-trimethoxy-8-[2',6'-dimethoxy-4'-(E)-propenylphenoxy]-phenylpropane, a neolignan isolated from Virola pavonis, and 25 of its synthetic analogues or correlated substances with ether linkage

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