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Benzaldehyde, 3,4-bis[2-[2-[2-[[(4-methylphenyl)sulfonyl]oxy]ethoxy]ethoxy]ethoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

209855-89-0

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209855-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209855-89-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,8,5 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 209855-89:
(8*2)+(7*0)+(6*9)+(5*8)+(4*5)+(3*5)+(2*8)+(1*9)=170
170 % 10 = 0
So 209855-89-0 is a valid CAS Registry Number.

209855-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-bis(2-{2-[2-(p-toluenesulfonyloxy)ethoxy]ethoxy}ethoxy)benzaldehyde

1.2 Other means of identification

Product number -
Other names 3,4-Bis(2-{2-[2-(2-p-toluenesulfonyloxy)ethoxy]ethoxy}ethoxy)benzaldehyde

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:209855-89-0 SDS

209855-89-0Relevant academic research and scientific papers

Supramolecular daisy chains

Cantrill,Youn,Stoddart,Williams

, p. 6857 - 6872 (2007/10/03)

Two series of self-complementary daisy chain monomers, in which a secondary ammonium ion-containing arm is grafted onto a macrocycle with either a [24]- or [25]crown-8 constitution, have been synthesized. In the solid- and 'gas'-phases, the parent [24]crown-8-based monomer forms dimeric superstructures, as revealed by X-ray crystallography and mass spectrometry, respectively. Elucidation of the complicated solution-phase behavior of this compound was facilitated by the synthesis and study of both deuterated, and fluorinated, analogues. These investigations revealed that the cyclic dimeric superstructure also dominates in solution, except when extremes of either concentration (low), temperature (high), or solvent polarity (highly polar, e.g., dimethyl sulfoxide) are employed. Whereas, upon aggregation, the [24]crown-8-based daisy chain monomers have the capacity to form stereoisomeric superstructures further complicating the study of this series of compounds. The assembly of [25]crown-8-based monomers gives only achiral superstructures. The weaker association exhibited between secondary dialkylammonium ions and crown ethers with a [25]crown-8 constitution, however, resulted in limited oligomerization-only dimeric and trimeric superstructures were formed at experimentally attainable concentrations-of [25]crown-8-based daisy chain monomers.

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