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17178-10-8

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17178-10-8 Usage

General Description

2-Methoxyethyl p-toluenesulfonate is a chemical compound commonly used as a mild, non-nucleophilic alkylating agent in organic synthesis. Also known as methyl p-toluenesulfonate, it is a clear, colorless liquid with a slight sweet odor. It is primarily utilized as an intermediate in the production of a variety of chemicals, including surfactants, pharmaceuticals, and dyes. It is also used as a solvent and as an additive in a variety of industrial and commercial products. Additionally, it is used as a protective agent in the synthesis of certain pharmaceuticals and as a stabilizer in the manufacturing of plastics and resins. Overall, 2-Methoxyethyl p-toluenesulfonate is a versatile chemical with a wide range of applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 17178-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,7 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17178-10:
(7*1)+(6*7)+(5*1)+(4*7)+(3*8)+(2*1)+(1*0)=108
108 % 10 = 8
So 17178-10-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O4S/c1-9-3-5-10(6-4-9)15(11,12)14-8-7-13-2/h3-6H,7-8H2,1-2H3

17178-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methoxyethyl 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names 2-METHOXYETHYL P-TOLUENESULFONATE

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:17178-10-8 SDS

17178-10-8Relevant articles and documents

2,3-Dihydro-2-methoxyethylimino-1,3-dimethylimidazole - A Novel Hemilabile Coordinating Chelate Ligand [1]

Kuhn, Norbert,Grathwohl, Martin,Nachtigal, Christiane,Steimann, Manfred

, p. 704 - 710 (2001)

The bifunctional 2,3-dihydro-2-methoxyethylimino-1,3-dimethylimidazole (C8H15N3O, 10) is obtained from the reaction of methoxyethyl tosylate (7) and 2,3-dihydro-2-imino-1,3-dimethylimidazole (8) followed by deprotonation i

Explorations of the solubilizing effectiveness of CH3OCH2CH2O substituents in the photocyclizations of some 1,2-diarylethylenes to [n]phenacenes

Bohen, Alyssa A.,Mullane, Kimberly C.,Bohen, Joseph M.,Mallory, Clelia W.,Mallory, Frank B.

, p. 3342 - 3345 (2015)

We have previously published many photocyclizations of 1,2-diarylethylenes to produce zig-zag aromatic ring systems with n = 5, 7, and 11 fused benzene rings. We invented the name [n]phenacenes for these compounds. To increase their solubilities we attach

PEG-modified aziridines for stereoselective synthesis of water-soluble fulleropyrrolidines

Kazakova, Angelina V.,Konev, Alexander S.,Zorin, Ivan M.,Poshekhonov, Igor S.,Korzhikov-Vlakh, Viktor A.,Khlebnikov, Alexander F.

, p. 9864 - 9873 (2019)

Diastereoselective synthesis of water-soluble fullerene compounds bearing a pharmacophore pyrrolofullerene-2′,5′-dicarboxylate unit is reported. The stereocontrol of the product configuration is achieved through stereospecificity of two consecutive concer

Designing Nonfullerene Acceptors with Oligo(Ethylene Glycol) Side Chains: Unraveling the Origin of Increased Open-Circuit Voltage and Balanced Charge Carrier Mobilities

Cui, Junjie,Park, Jung-Hwa,Kim, Dong Won,Choi, Min-Woo,Chung, Hae Yeon,Kwon, Oh Kyu,Kwon, Ji Eon,Park, Soo Young

supporting information, p. 2481 - 2488 (2021/07/26)

Despite the recent rapid development of organic solar cells (OSCs), the low dielectric constant (?r=3–4) of organic semiconducting materials limits their performance lower than inorganic and perovskite solar cells. In this work, we introduce oligo(ethylene glycol) (OEG) side chains into the dicyanodistyrylbenzene-based non-fullerene acceptors (NIDCS) to increase its ?r up to 5.4. In particular, a NIDCS acceptor bearing two triethylene glycol chains (NIDCS-EO3) shows VOC as high as 1.12 V in an OSC device with a polymer donor PTB7, which is attributed to reduced exciton binding energy of the blend film. Also, the larger size grain formation with well-ordered stacking structure of the NIDCS-EO3 blend film leads to the increased charge mobility and thus to the improved charge mobility balance, resulting in higher JSC, FF, and PCE in the OSC device compared to those of a device using the hexyl chain-based NIDCS acceptor (NIDCS-HO). Finally, we fabricate NIDCS-EO3 devices with various commercial donors including P3HT, DTS-F, and PCE11 to show higher photovoltaic performance than the NIDCS-HO devices, suggesting versatility of NIDCS-EO3.

Styryl xanthine derivatives and uses thereof (by machine translation)

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Paragraph 0174; 0176; 0177; 0178; 0179, (2019/08/02)

The invention discloses styryl xanthine derivatives and application, and particularly, relates to a novel styryl xanthine derivative and a pharmaceutical composition containing the same, and can be used as selective adenosine A. 2A Are antagoni

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