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17078-61-4

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17078-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17078-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,7 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17078-61:
(7*1)+(6*7)+(5*0)+(4*7)+(3*8)+(2*6)+(1*1)=114
114 % 10 = 4
So 17078-61-4 is a valid CAS Registry Number.

17078-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 4,5-dimethoxybenzene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names x-<14C>-Metahemipinsaeure-dimethylester

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:17078-61-4 SDS

17078-61-4Relevant articles and documents

Synthesis of Core-Modified Third-Generation Light-Driven Molecular Motors

Berrocal, José Augusto,Pfeifer, Lukas,Heijnen, Dorus,Feringa, Ben L.

, p. 10670 - 10680 (2020/09/18)

The synthesis and characterization of a series of light-driven third-generation molecular motors featuring various structural modifications at the central aromatic core are presented. We explore a number of substitution patterns, such as 1,2-dimethoxybenzene, naphthyl, 1,2-dichlorobenzene, 1,1′:2′,1″-terphenyl, 4,4″-dimethoxy-1,1':2′,1″-terphenyl, and 1,2-dicarbomethoxybenzene, considered essential for designing future responsive systems. In many cases, the synthetic routes for both synthetic intermediates and motors reported here are modular, allowing for their post-functionalization. The structural modifications introduced in the core of the motors result in improved solubility and a bathochromic shift of the absorption maxima. These features, in combination with a structural design that presents remote functionalization of the stator with respect to the fluorene rotors, make these novel motors particularly promising as light-responsive actuators in covalent and supramolecular materials.

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