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37860-51-8

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37860-51-8 Usage

Description

TETRAETHYLENE GLYCOL DI-P-TOSYLATE, also known as Tos-PEG5-Tos, is a PEG (Polyethylene Glycol) linker containing two tosyl groups. It is characterized by its hydrophilic PEG spacer, which enhances solubility in aqueous media, and the tosyl group, which acts as an excellent leaving group for nucleophilic substitution reactions.

Uses

Used in Chemical Sensing Applications:
TETRAETHYLENE GLYCOL DI-P-TOSYLATE is used as a component in the preparation of donor-spacer-acceptor podand systems, which serve as dual channel fluorosensors for detecting Li+, Mg2+, and Ca2+ ions. The unique properties of the Tos-PEG5-Tos molecule, including its hydrophilic PEG spacer and tosyl leaving group, contribute to the effective detection and differentiation of these ions in various applications.
Used in Chemical Research and Development:
In the field of chemical research and development, TETRAETHYLENE GLYCOL DI-P-TOSYLATE is utilized for its ability to facilitate nucleophilic substitution reactions due to the presence of the tosyl group. This makes it a valuable tool in the synthesis of various chemical compounds and materials.
Used in Pharmaceutical and Biomedical Applications:
The hydrophilic nature of the PEG spacer in TETRAETHYLENE GLYCOL DI-P-TOSYLATE makes it a potential candidate for use in the development of drug delivery systems and other biomedical applications. Its solubility in aqueous media can be advantageous for the design of biocompatible materials and formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 37860-51-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,8,6 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 37860-51:
(7*3)+(6*7)+(5*8)+(4*6)+(3*0)+(2*5)+(1*1)=138
138 % 10 = 8
So 37860-51-8 is a valid CAS Registry Number.
InChI:InChI=1/C22H30O9S2/c1-19-3-7-21(8-4-19)32(23,24)30-17-15-28-13-11-27-12-14-29-16-18-31-33(25,26)22-9-5-20(2)6-10-22/h3-10H,11-18H2,1-2H3

37860-51-8 Well-known Company Product Price

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  • Aldrich

  • (341703)  Tetraethyleneglycoldi(p-toluenesulfonate)  97%

  • 37860-51-8

  • 341703-10G

  • 762.84CNY

  • Detail
  • Aldrich

  • (341703)  Tetraethyleneglycoldi(p-toluenesulfonate)  97%

  • 37860-51-8

  • 341703-50G

  • 2,558.79CNY

  • Detail

37860-51-8Relevant articles and documents

Dynamic host-guest interaction enables autonomous single molecule blinking and super-resolution imaging

Sasmal, Ranjan,Das Saha, Nilanjana,Schueder, Florian,Joshi, Divyesh,Sheeba, Vasu,Jungmann, Ralf,Agasti, Sarit S.

, p. 14430 - 14433 (2019)

Synthetic host-guest complexes are inherently dynamic as they employ weak and reversible noncovalent interactions for their recognition processes. We strategically exploited dynamic supramolecular recognition between fluorescently labeled guest molecules to complementary cucurbit[7]uril hosts to obtain stochastic switching between fluorescence ON- and OFF-states, enabling PAINT-based nanoscopic imaging in cells and tissues.

Facile synthesis of a polyether-tethered dimeric berberine as a highly effective DNA-cleaving agent in the presence of Cu(ii) ion

Wang, Yong-Min,Zhou, Chun-Qiong,Chen, Jin-Xiang,Lin, Yan-Ling,Zeng, Wei,Kuang, Bi-Cheng,Fu, Wei-Long,Chen, Wen-Hua

, p. 1400 - 1404 (2013)

A polyether-tethered dimeric berberine was synthesized and found to be capable of efficiently converting pBR322 DNA into open circular and linear forms in the presence of Cu(ii) ions under physiological conditions, most probably via an oxidative mechanism

Biscrown-annulated TTFAQ-dianthracene hybrid: Synthesis, structure, and metal ion sensing

Shao, Min,Dongare, Prateek,Dawe, Louise N.,Thompson, David W.,Zhao, Yuming

, p. 3050 - 3053 (2010)

A new fluorescence chemosensor (3) made up of a biscrown-annulated TTFAQ receptor and two anthracene fluorophores was designed and synthesized. Its solid-state structure was disclosed by X-ray crystallographic analysis, while fluorescence titrations indic

Chiral synthesis via organoboranes. 46. An efficient preparation of chiral pyridino- and thiopheno-18-crown-6 ligands from enantiomerically pure C2-symmetric pyridine- and thiophenediols

Chen, Guang-Ming,Brown, Herbert C.,Ramachandran, P. Veeraraghavan

, p. 721 - 725 (1999)

Asymmetric reduction of 2,6-diacylpyridines with B- chlorodiisopinocampheylborane provides the corresponding C2-symmetric diols in very high de and ee. Asymmetric allylboration of 2,6- pyridinedicarboxaldehyde and 2,5-thiophenedicarboxaldehyde

Enhancement of intramolecular photocycloaddition of bichromophoric compounds via inclusion in low-density polyethylene films

Tung, Chen-Ho,Yuan, Zhen-Yu,Wu, Li-Zhu,Wiess, Richard G.

, p. 5156 - 5161 (1999)

The photocycloaddition of tetra- and penta(ethylene glycol) labeled at the chain terminals with 2-naphthoyl groups (N-P(n)-N; n = 4 or 5) and tetra(ethylene glycol) terminated by 7-(4-methylcoumarinyl) groups (C-P4-C) has been investigated in h

Design, synthesis and biological evaluation of a halogenated phenazine-erythromycin conjugate prodrug for antibacterial applications

Yang, Hongfen,Liu, Ke,Jin, Shouguang,Huigens III, Robert W.

supporting information, p. 1483 - 1487 (2021/03/01)

There is a significant need for new antibacterial agents as pathogenic bacteria continue to threaten human health through the acquisition of resistance and tolerance towards existing antibiotics. Over the last several years, our group has been developing

Unraveling the anti-influenza effect of flavonoids: Experimental validation of luteolin and its congeners as potent influenza endonuclease inhibitors

Albi?ana, Carlos Berenguer,Brynda, Ji?í,Fanfrlík, Jind?ich,Flieger, Miroslav,Hodek, Jan,Karlukova, Elena,Ko?í?ek, Milan,Konvalinka, Jan,Machara, Ale?,Majer, Pavel,Radilová, Kate?ina,Weber, Jan,Zima, Václav

supporting information, (2020/09/09)

The biological effects of flavonoids on mammal cells are diverse, ranging from scavenging free radicals and anti-cancer activity to anti-influenza activity. Despite appreciable effort to understand the anti-influenza activity of flavonoids, there is no clear consensus about their precise mode-of-action at a cellular level. Here, we report the development and validation of a screening assay based on AlphaScreen technology and illustrate its application for determination of the inhibitory potency of a large set of polyols against PA N-terminal domain (PA-Nter) of influenza RNA-dependent RNA polymerase featuring endonuclease activity. The most potent inhibitors we identified were luteolin with an IC50 of 72 ± 2 nM and its 8-C-glucoside orientin with an IC50 of 43 ± 2 nM. Submicromolar inhibitors were also evaluated by an in vitro endonuclease activity assay using single-stranded DNA, and the results were in full agreement with data from the competitive AlphaScreen assay. Using X-ray crystallography, we analyzed structures of the PA-Nter in complex with luteolin at 2.0 ? resolution and quambalarine B at 2.5 ? resolution, which clearly revealed the binding pose of these polyols coordinated to two manganese ions in the endonuclease active site. Using two distinct assays along with the structural work, we have presumably identified and characterized the molecular mode-of-action of flavonoids in influenza-infected cells.

Bioorthogonal Ligation and Cleavage by Reactions of Chloroquinoxalines with ortho-Dithiophenols

Fu, Hua,Li, Hongyun,Li, Youshan,Lou, Zhenbang,Yang, Haijun,Zhao, Yufen

supporting information, p. 3671 - 3677 (2020/02/04)

A bioorthogonal ligation and cleavage method via reactions of chloroquinoxalines (CQ) and ortho-dithiophenols (DT) is presented. Double nucleophilic substitutions of ortho-dithiophenols to chloroquinoxalines provide conjugates containing tetracyclic benzo[5,6][1,4]dithiino[2,3-b]quinoxaline with strong built-in fluorescence together with release of the other functional molecules. Three cleavable linkers were designed and successfully used in release of the molecules containing biotin from the protein conjugates. The CQ-DT bioorthogonal reactions can be applied for the bioorthogonal ligations, bioorthogonal cleavages, and trans-tagging of proteins, and show advantages of readily accessible unnatural orthogonal groups, appealing reaction kinetics (k2≈1.3 m?1 s?1), excellent biocompatibility of orthogonal groups, and high stability of conjugates. This complements previous bioorthogonal reactions and is a new route for protein-fishing applications and in-gel fluorescence analysis.

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