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Naphtho[1,8-de][1,3]dithiine is a heterocyclic organic compound characterized by a naphthalene core with two sulfur atoms incorporated into the structure, forming a dithiine ring. naphtho[1,8-de][1,3]dithiine is notable for its unique electronic properties and potential applications in materials science, particularly in the development of organic semiconductors and conductive polymers. The presence of sulfur atoms in the molecule can significantly influence its electronic structure, making it a subject of interest for researchers exploring new materials with tailored properties for use in electronics and energy storage devices.

204-14-8

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204-14-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 204-14-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,0 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 204-14:
(5*2)+(4*0)+(3*4)+(2*1)+(1*4)=28
28 % 10 = 8
So 204-14-8 is a valid CAS Registry Number.

204-14-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Naphtho[1,8-de]-1,3-dithiin

1.2 Other means of identification

Product number -
Other names naphtho<1,8-de>-1,3-dithiin

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:204-14-8 SDS

204-14-8Downstream Products

204-14-8Relevant academic research and scientific papers

Syntheses and Properties of 2,2'-Binaphtho-1,3-dithiinylidene and Its Selenium Analog, 2-(1,3-Dithiol-2-ylidene)naphtho-1,3-dithiin, and 2-(4H-Thiopyran-4-ylidene)naphtho-1,3-dithiin

Yui, Koji,Aso, Yoshio,Otsubo, Tetsuo,Ogura, Fumio

, p. 953 - 960 (1988)

In order to discover new electron donors for conducting charge-transfer complexes, the four title compounds 1-4 composed of two heterocycles have been prepared via 1,8-dichalcogen-bridged naphthalene.The cyclic voltammetery indicates that symmetrical 1 and 2 are poor donors, but unsymmetrical 3 and 4 possess considerable donor abilities.The latter compounds are thus capable of forming some crystalline charge-transfer complexes with strong acceptors such as TCNQ, TCNQF4, and DDQ, which are, however, semi-conducting.

SYNTHESES AND PROPERTIES OF BINAPHTHO-1,3-DITHIIN-2-YLIDENE AND ITS SELENIUM ANALOGUE

Yui, Koji,Aso, Yoshio,Otsubo, Tetsuo,Ogura, Fumio

, p. 551 - 554 (1986)

With view to discovering new electron donors for low-dimensionally metallic materials, the title compounds were prepared via the corresponding 1,8-dichalcogen-bridged naphthalenes.Their donor characters were examined by cyclic voltammetry, as compared with those of the reference compounds.

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