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26150-06-1

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26150-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26150-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,5 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26150-06:
(7*2)+(6*6)+(5*1)+(4*5)+(3*0)+(2*0)+(1*6)=81
81 % 10 = 1
So 26150-06-1 is a valid CAS Registry Number.

26150-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-[2-(2-prop-2-enoxyethoxy)ethoxy]ethoxy]ethanol

1.2 Other means of identification

Product number -
Other names 2-(2-(2-(2-allyloxy-ethoxy)-ethoxy)-ethoxy)-ethanol

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:26150-06-1 SDS

26150-06-1Relevant articles and documents

Design of functionalized cellulosic honeycomb films: Site-specific biomolecule modification via "click chemistry"

Xu, William Z.,Zhang, Xinyue,Kadla, John F.

, p. 350 - 357 (2012)

Value-added materials from naturally abundant polymers such as cellulose are of significant importance. In particular, cellulosic open-framework structures with controlled chemical functionality of the internal surface have great potential in many biosens

Stereoselective synthesis of a topologically chiral molecule: The trefoil knot

Perret-Aebi, Laure-Emmanuelle,Von Zelewsky, Alexander,Dietrich-Buchecker, Christiane,Sauvage, Jean-Pierre

, p. 4482 - 4485 (2004)

Tying nice neat knots is demonstrated on a molecular level with the stereoselective synthesis of a trefoil knot. The key reaction was the completely stereoselective formation of a double-stranded helical precursor from two pinene-bipyridine threads around two CuI centers (the pinene moieties contain stereogenic centers). The helix was then transformed through several steps into 1; demetallation of the complex 1 yielded the configurationally predetermined free trefoil knot.

NOVEL TRIAZINE COMPOUND, ALL-SOLID-STATE POLYMER ELECTROLYTE COMPOSITION AND USE THEREOF

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Paragraph 0123; 0139-0142, (2018/04/12)

The present invention relates to a novel triazine compound represented by chemical formula 1, an all-solid-state polymer electrolyte composition comprising the same as a cross-linking agent and uses thereof. More specifically, the triazine compound effectively inhibits crystallization of a plasticizer at a low temperature (room temperature) to show significantly improved ion conductivity, and can realize significantly improved electrochemical stability and excellent battery properties, thereby being usefully used as an all-solid-state polymer electrolyte composition such as a lithium-polymer secondary battery, a dye-sensitized solar cell, etc.COPYRIGHT KIPO 2018

TAU-PROTEIN TARGETING PROTACS AND ASSOCIATED METHODS OF USE

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Paragraph 1461, (2018/05/24)

The present disclosure relates to bifunctional compounds, which find utility as modulators of tau protein. In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a VHL or cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds tau protein, such that tau protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of tau. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of tau protein. Diseases or disorders that result from aggregation or accumulation of tau protein are treated or prevented with compounds and compositions of the present disclosure.

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