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Aethylenglykol-octylaether-benzylaether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93541-24-3

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93541-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93541-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,5,4 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 93541-24:
(7*9)+(6*3)+(5*5)+(4*4)+(3*1)+(2*2)+(1*4)=133
133 % 10 = 3
So 93541-24-3 is a valid CAS Registry Number.

93541-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-octoxyethoxymethylbenzene

1.2 Other means of identification

Product number -
Other names Aethylenglykol-octylaether-benzylaether

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:93541-24-3 SDS

93541-24-3Downstream Products

93541-24-3Relevant academic research and scientific papers

Synthesis and antiproliferative activity of alkylphosphocholines

Agresta, Mandy,D'Arrigo, Paola,Fasoli, Ezio,Losi, Daniele,Pedrocchi-Fantoni, Giuseppe,Riva, Simona,Servi, Stefano,Tessaro, Davide

, p. 201 - 210 (2007/10/03)

Alkylphosphocholines (APC) with one or more methylene groups in the alkyl chain replaced by oxygen atoms or carbonyl groups, or both have been assembled modularly using ω-diols as central building blocks. Out of 25 new compounds of this kind, 11 were evaluated for their antiproliferative activity on four cell lines and compared with miltefosine to evaluate their hemolytic activity (HA) and cytotoxicity on non-tumoral cells (MT2), used as markers of adverse effects. Compound 13 was more active on cancer cell lines than on non-tumoral cells and the data were similar for MTT and thymidine incorporation assays. It had less HA than miltefosine. Compound 13 could therefore be a candidate for the preparation of compounds with higher cytotoxicity on cancer cells and lower general toxicity.

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