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Benzoic acid, 3,5-bis[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

288850-03-3

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288850-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 288850-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,8,5 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 288850-03:
(8*2)+(7*8)+(6*8)+(5*8)+(4*5)+(3*0)+(2*0)+(1*3)=183
183 % 10 = 3
So 288850-03-3 is a valid CAS Registry Number.

288850-03-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-bis-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-benzoic acid methyl ester

1.2 Other means of identification

Product number -
Other names Methyl 3,5-bis(methoxyethoxyethoxyethoxy)benzoate

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:288850-03-3 SDS

288850-03-3Relevant academic research and scientific papers

Construction of Janus dendrimers through a self-assembly approach involving chiral discrimination at a focal point

Cole, Ashley M.,Kilway, Kathleen V.,Menuey, Elizabeth M.,Moteki, Shin A.,Zhou, John

supporting information, p. 6404 - 6407 (2021/07/02)

A strategy to build Janus dendrimersviathe chirality-directed self-assembly of heteroleptic Zn(ii) BOX complexes is reported. The method allows quantitative synthesis of Janus dendrimersin situwithout the need for purifications. Each dendritic domain of t

Self-assembly of uncharged amphiphilic porphyrins and incorporation of C60 fullerenes in water

Jung, Su Hee,Lee, Ji-Won,Kim, Hee-Joon

, p. 634 - 639 (2016/06/09)

We synthesised an uncharged amphiphilic porphyrin, meso-tetrakis-(3,5-di-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-phenyl)-porphyrin, and investigated the supramolecular self-assembly of the porphyrins and the incorporation of C60 molecules into

Synthesis, structural characterization, and thermoresponsivity of hybrid supramolecular dendrimers bearing a polyoxometalate core

Chen, Hailong,Yang, Yang,Wang, Yizhan,Wu, Lixin

, p. 11051 - 11061 (2013/09/02)

A series of cationic dendrons bearing triethylene glycol monomethyl ether terminal groups of different generations have been synthesized and used to encapsulate an inorganic polyanionic cluster [K12.5Na 1.5(NaP5W30O110)] through electrostatic interactions. The resulting dendritic cation-encapsulated polyoxometalate (POM) complexes, cluster-dendrimers, are soluble in water and exhibit lower critical solution temperatures (LCST). The thermoresponsivities of these complexes in aqueous solutions were studied by turbidimetry and variable-temperature 1H NMR spectroscopy. The observed cloud points show a remarkable dependence on the generation of the dendrons. Complexes composed of first-generation dendrons exhibit no obvious thermoresponsive properties, but for complexes bearing second-generation dendrons, the LCST decreases as the number of dendritic cations around the POM cluster increases. Complexes composed of third-generation cations underwent reversible aggregation and disaggregation upon heating and cooling, respectively. This thermally induced self-aggregation was characterized by DLS and TEM. In addition, the effects of salt and solvent on the LCST were investigated. This research demonstrates a new type of thermoresponsive dendritic organic-inorganic hybrid complex and provides a general route to the endowment of POMs with temperature-sensitive properties through electrostatic interactions.

Methyl pyropheophorbide-a analogues: Potential fluorescent probes for the peripheral-type benzodiazepine receptor. Effect of central metal in photosensitizing efficacy

Chen, Yihui,Zheng, Xiang,Dobhal, Mahabeer P.,Gryshuk, Amy,Morgan, Janet,Dougherty, Thomas J.,Oseroff, Allan,Pandey, Ravindra K.

, p. 3692 - 3695 (2007/10/03)

Pyropheophorbides and their metal complexes were synthesized to investigate their applications as nonradioactive peripheral benzodiazepine receptor (PBR) binding probes and photosensitizers for use in photodynamic therapy. They were found to be localized in mitochondria and showed significant binding to PBR. In some cases, the PBR binding values were similar to that for 17 (PK11195, 1-(2-chlorophenyl)-N-methyl-N-(1-methylpropyl)isoquinoline-3-carboxamide). However, no direct correlation between 17 displacement ability and photosensitizing efficacy of photosensitizers was observed.

Phthalocyanine-centred and naphthalocyanine-centred aryl ether dendrimers with oligo(ethyleneoxy) surface groups

Brewis, Matthew,Helliwell, Madeleine,McKeown, Neil B.

, p. 3863 - 3872 (2007/10/03)

The synthesis of the 1st, 2nd and 3rd generation phthalocyanine-centred and naphthalocyanine-centred poly(aryl ether) dendrimers possessing oligo(ethyleneoxy) surface groups is described. These materials are soluble in polar protic solvents. For both type

Fullerodendrimers with peripheral triethyleneglycol chains

Rio, Yannick,Nicoud, Jean-Fran?ois,Rehspringer, Jean-Luc,Nierengarten, Jean-Fran?ois

, p. 10207 - 10210 (2007/10/03)

Triethylene glycol terminated poly(aryl ether) dendritic branches with an aldehyde function at the focal point have been prepared and attached to C60 by a 1,3-dipolar cycloaddition. (C) 2000 Elsevier Science Ltd.

Synthesis and characterisation of water-soluble poly(aryl ether) dendrimers for encapsulation of biomimetic active site analogues

Hannon, Michael J.,Mayers, Paul C.,Taylor, Paul C.

, p. 1881 - 1889 (2007/10/03)

Synthetic strategies to incorporate active site analogues of metalloenzymes at the core of water-soluble dendritic structures are explored. Synthesis of water-soluble aryl ether dendrimers containing tripyridyl metal-binding sites is successful when a con

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