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255-50-5

1,4-Benzodithiin is a heterocyclic organic compound with the chemical formula C8H6S2. It features a benzene ring fused to two dithiin rings, which are composed of sulfur atoms and carbon atoms in a cyclic structure. 1,4-Benzodithiin is known for its unique electronic properties and potential applications in materials science, particularly in the development of organic semiconductors and conductive polymers. Due to its sulfur-containing structure, 1,4-Benzodithiin can also be explored for its reactivity and stability in various chemical transformations.

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  • 255-50-5 Structure

  • Basic information

    1. Product Name: 1,4-Benzodithiin
    2. Synonyms:
    3. CAS NO:255-50-5
    4. Molecular Formula: C8H6S2
    5. Molecular Weight: 166.26300
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 255-50-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,4-Benzodithiin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,4-Benzodithiin(255-50-5)
    11. EPA Substance Registry System: 1,4-Benzodithiin(255-50-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 255-50-5(Hazardous Substances Data)

255-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 255-50-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,5 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 255-50:
(5*2)+(4*5)+(3*5)+(2*5)+(1*0)=55
55 % 10 = 5
So 255-50-5 is a valid CAS Registry Number.

255-50-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-benzodithiine

1.2 Other means of identification

Product number -
Other names 1,4-Benzodithiin

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:255-50-5 SDS

255-50-5Relevant articles and documents

Synthesis and Diels-Alder reactions of enantiopure (-)-trans-benzo[d]-dithuene-S,S′-dioxide

Cecchet, Elisa,Di Furia, Fulvio,Licini, Giulia,Modena, Giorgio

, p. 369 - 372 (1996)

Enantiopure (-)-trans-benzo[d]dithiine-S,S′-dioxide 4 was obtained by enantioselective oxidation of the parent benzo[d]dithiine. The reaction of the bis-sulfoxide with a series of cyclic dienes affords the corresponding Diels-Alder cycloadducts with diastereoselectivities ranging from fair to high and good chemical yields.

Synthesis of unsaturated 1,4-heteroatom-containing benzo-fused heterocycles using a sequential isomerization-ring-closing metathesis strategy

Morgans, Garreth L.,Ngidi, E. Lindani,Madeley, Lee G.,Khanye, Setshaba D.,Michael, Joseph P.,de Koning, Charles B.,van Otterlo, Willem A.L.

experimental part, p. 10650 - 10659 (2010/01/16)

A small library of 1,4-benzodioxins and 4H-1,4-benzoxazines was synthesized from the corresponding bis-allyloxy precursors by way of an initial isomerization to the bis-vinyloxy compounds, followed by a ring-closing metathesis using the second generation Grubbs' catalyst (G2). A related strategy, starting from benzene-1,2-dithiol and 2-mercaptophenol, afforded benzodithiin and 1,4-benzoxathiin, respectively.

1,4-BENZODITHIIN 1,1,4,4,-TETRAOXIDE AS DIENOPHILE

Nakayama, Juzo,Nakamura, Yoichi,Hoshino, Masamatsu

, p. 1119 - 1122 (2007/10/02)

1,4-Benzodithiin 1,1,4,4,-tetraoxide undergoes the Diels-Alder reaction with a series of dienes under mild condition to provide the corresponding adducts in excellent yields.The adduct with anthracene is desulfonated to afford dibenzobarrelene, thus showi

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