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118591-58-5

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118591-58-5 Usage

General Description

Ethanol, 2-(2-hydroxyethoxy)-, 1-(4-methylbenzenesulfonate), also known as ethylene glycol monomethyl ether sulfate, is a chemical compound used primarily as a surfactant in various industrial and household products such as detergents, cleaners, and personal care items. It is a clear, colorless liquid with a slightly sweet odor. This chemical is considered to be relatively safe for use in these products when handled properly, and it has low volatility and low potential for toxicity. However, it is important to follow proper handling and safety guidelines when working with this chemical to avoid any potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 118591-58-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,9 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 118591-58:
(8*1)+(7*1)+(6*8)+(5*5)+(4*9)+(3*1)+(2*5)+(1*8)=145
145 % 10 = 5
So 118591-58-5 is a valid CAS Registry Number.

118591-58-5Relevant articles and documents

Clickable prodrugs bearing potent and hydrolytically cleavable nicotinamide phosphoribosyltransferase inhibitors

Sadrerafi, Keivan,Mason, Emilia O.,Lee, Mark W.

, p. 987 - 995 (2018)

Purpose: Our previous study indicated that carborane containing small-molecule 1-(hydroxymethyl)-7-(4′-(trans-3″-(3′″-pyridyl)acrylamido)butyl)-1,7-dicarbadodecaborane (hm-MC4-PPEA), was a potent inhibitor of nicotinamide phosphoribosyltransferase (Nampt)

Gold nanoparticles coated with semi-fluorinated oligo(ethylene glycol) produce sub-100 nm nanoparticle vesicles without templates

Niikura, Kenichi,Iyo, Naoki,Higuchi, Takeshi,Nishio, Takashi,Jinnai, Hiroshi,Fujitani, Naoki,Ijiro, Kuniharu

, p. 7632 - 7635 (2012)

Gold nanoparticles (NPs) with diameters of 5, 10, and 20 nm coated with semifluorinated oligo(ethylene glycol) ligands were formed into sub-100 nm hollow NP assemblies (NP vesicles) in THF without the use of a template. The NP vesicles maintained their st

Synthesis of optically active 1,1′-binaphthyl-phthalocyanines linked via a crown ether unit

Liu, Hong-Wei,Chen, Chuan-Fu,Ai, Min,Gong, Ai-Jun,Jiang, Jing,Xi, Fu

, p. 4915 - 4922 (2000)

Novel optically active metal and metal-free phthalocyanines, substituted with 1,1′-binaphthyl crown ether units, have been synthesized and characterized.

Closing the Loop: Triazolylpyridine Coordination Drives the Self-Assembly of Metallomacrocycles with Tunable Topologies for Small-Molecule and Guanine-Quadruplex Recognition

Miron, Caitlin E.,Colden Leung, Madelaine R.,Kennedy, Emily I.,Fleischel, Olivier,Khorasani, Mona Ashraf,Wu, Nan,Mergny, Jean-Louis,Petitjean, Anne

, p. 18718 - 18734 (2018)

The 2-(1,2,3-triazol-4-yl)pyridine motif, with its facile “click” synthesis and remarkable coordinative properties, is an attractive chelate for applications in the metal-directed self-assembly of intricate three-dimensional structures. Organic ligands th

SYNTHESIS OF 2-(2-AMINOETHOXY) ETHANOL

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Paragraph 0055-0057, (2021/02/12)

A method for synthesizing 2-(2-aminoethoxy) ethanol, including the steps of producing 2-(2-phthalimidoethoxy) ethanol by reacting 5-tosyloxy-3-oxapentanol with potassium phthalate and converting the 2-(2-phthalimidoethoxy) ethanol to the 2-(2-aminoethoxy) ethanol by reacting the 2-(2-phthalimidoethoxy) ethanol with hydrazine monohydrate. Reacting the 2-(2-phthalimidoethoxy) ethanol with the hydrazine monohydrate may include forming a final mixture by adding the hydrazine monohydrate to a solution of 2-(2-phthalimidoethoxy) ethanol, refluxing the final mixture in a nitrogen atmosphere, extracting a second organic phase containing the 2-(2-aminoethoxy) ethanol from the final mixture using a second portion of chloroform, and purifying the 2-(2-aminoethoxy) ethanol from the second organic phase.

Synthesis, biological evaluation and QSAR studies of new thieno[2,3-d]pyrimidin-4(3H)-one derivatives as antimicrobial and antifungal agents

Magoulas, George E.,Kalopetridou, Lefkothea,?iri?, Ana,Kritsi, Eftichia,Kouka, Paraskevi,Zoumpoulakis, Panagiotis,Chondrogianni, Niki,Sokovi?, Marina,Prousis, Kyriakos C.,Calogeropoulou, Theodora

, (2020/12/13)

A series of new thieno[2,3-d]pyrimidin-4(3H)-one derivatives were synthesized and evaluated for their activity against four gram-positive and four gram-negative bacterial and eight fungal species. The majority of the compounds exhibited excellent antimicr

COMPOUNDS AND USES THEREOF

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Page/Page column 157, (2021/08/06)

The present disclosure features compounds and methods useful for the treatment of BAF complex-related disorders.

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