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248588-29-6

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248588-29-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 248588-29-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,8,5,8 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 248588-29:
(8*2)+(7*4)+(6*8)+(5*5)+(4*8)+(3*8)+(2*2)+(1*9)=186
186 % 10 = 6
So 248588-29-6 is a valid CAS Registry Number.

248588-29-6Downstream Products

248588-29-6Relevant academic research and scientific papers

Hierarchical self-assembly of all-organic photovoltaic devices

Huang, Chih-Hao,McClenaghan, Nathan D.,Kuhn, Alexander,Bravic, Georges,Bassani, Dario M.

, p. 2050 - 2059 (2006)

Photovoltaic devices built by a hierarchical self-assembly process using hydrogen-bonding terminated self-assembled monolayers (SAMs) on gold and the combination of a hydrogen-bonding barbituric acid appended fullerene and a complementary melamine termina

CELL IMPERMEABLE COELENTERAZINE ANALOGUES

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Paragraph 0201-0203, (2018/06/15)

Described are coelenterazine analogues, methods for making the analogues, kits comprising the analogues, and methods of using the compounds for the detection of luminescence in luciferase-based assays.

Hydrogen-bonded CdS nanoparticle assemblies on electrodes for photoelectrochemical applications

Baron, Ronan,Huang, Chih-Hao,Bassani, Dario M.,Onopriyenko, Avital,Zayats, Maya,Willner, Itamar

, p. 4010 - 4015 (2007/10/03)

(Chemical Equation Presented) Trapping the light fantastic-ally! Enhanced photocurrents are observed for hydrogen-bonded gold nanoparticle/CdS nanoparticle arrays associated with a gold electrode surface (see scheme) as a result of charge separation and c

Solid- and solution-phase synthesis of vancomycin and vancomycin analogues with activity against vancomycin-resistant bacteria

Nicolaou,Cho, Suk Young,Hughes, Robert,Winssinger, Nicolas,Smethurst, Christian,Labischinski, Harald,Endermann, Rainer

, p. 3798 - 3823 (2007/10/03)

Vancomycin, the prototypical member of the glycopeptide family of antibiotics, is a clinically used antibiotic employed against a variety of drug-resistant bacterial strains including methicillin-resistant Staphylococcus aureus (MRSA). The recent emergence of vancomycin resistance, viewed as a growing threat to public health, prompted us to initiate a program aimed at restoring the potency of this important antibiotic through chemical manipulation of the vancomycin structure. Herein, we describe the development of synthetic technology based on the design of a novel selenium safety catch linker, application of this technology to a solid-phase semisynthesis of vancomycin, and the solid- and solution-phase synthesis of vancomycin libraries. Biological evaluation of these compound libraries led to the identification of a number of in vitro highly potent antibacterial agents effective against vancomycin-resistant bacteria. In addition to aiding these investigations, the solid-phase chemistry described herein is expected to enhance the power of combinatorial chemistry and facilitate chemical biology and medicinal chemistry studies.

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