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925674-61-9

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925674-61-9 Usage

Description

Pyridine, 2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-5-yl)is a heterocyclic aromatic compound belonging to the class of pyridines, featuring a unique fused thieno-dioxin ring system. This chemical is recognized for its potential applications in various fields due to its distinctive structure and reactivity.

Uses

Used in Organic Synthesis:
Pyridine, 2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-5-yl)is utilized as a solvent, reagent, and building block in organic synthesis, contributing to the creation of diverse chemical compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, this compound is studied for its potential applications, given its unique structure and reactivity, which may contribute to the development of new drugs.
Used in Agrochemical Industry:
Pyridine, 2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-5-yl)is also being investigated for its possible use in agrochemicals, where its properties could be harnessed to develop novel pesticides or other agricultural products.
Used in Coordination Chemistry:
Pyridine, 2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-5-yl)has been examined for its role as a ligand in coordination chemistry, which could lead to advances in the design of metal complexes with specific properties and applications.
Used in Synthesis of Functional Materials:
Pyridine, 2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-5-yl)is considered as a precursor in the synthesis of various functional materials, where its incorporation can lead to the development of new materials with unique characteristics.
Further research is necessary to fully explore the potential and applications of Pyridine, 2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-5-yl)-, as its multifaceted utility across different industries holds promise for future discoveries and innovations.

Check Digit Verification of cas no

The CAS Registry Mumber 925674-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,5,6,7 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 925674-61:
(8*9)+(7*2)+(6*5)+(5*6)+(4*7)+(3*4)+(2*6)+(1*1)=199
199 % 10 = 9
So 925674-61-9 is a valid CAS Registry Number.

925674-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)pyridine

1.2 Other means of identification

Product number -
Other names Pyridine,2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-5-yl)

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:925674-61-9 SDS

925674-61-9Downstream Products

925674-61-9Relevant articles and documents

Novel chromophores from alternated pyridine-ethylenedioxythiophene unit oligomers: Dramatic enhancement of photoluminescence properties in elongated derivatives

Chevallier, Floris,Charlot, Marina,Katan, Claudine,Mongin, Florence,Blanchard-Desce, Mireille

, p. 692 - 694 (2009)

Novel chromophores based on the alternation of electron-poor (pyridyl) and electron-rich (ethylenedioxythienyl) heterocycles were synthesized for the first time and shown to exhibit attractive optical properties in relation with their specific electronic and geometrical (coiled structure) features. The Royal Society of Chemistry 2009.

Synthesis of mono- and bis-arylated 3,4-(ethylenedioxythiophenes) via direct palladium catalyzed arylation reactions

Mohanakrishnan, Arasambattu K.,Amaladass,Arul Clement

, p. 539 - 544 (2007/10/03)

The synthesis of arylated/heteroarylated 3,4-ethylenedioxythiophene derivatives is reported using a straightforward palladium mediated Heck coupling of 3,4-ethylenedioxythiophene with various aryl/heteroaryl halides.

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