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  • 16259-99-7 Structure
  • Basic information

    1. Product Name: Octafluoroselenanthrene
    2. Synonyms: Octafluoroselenanthrene
    3. CAS NO:16259-99-7
    4. Molecular Formula: C12F8Se2
    5. Molecular Weight: 454.04
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16259-99-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Octafluoroselenanthrene(CAS DataBase Reference)
    10. NIST Chemistry Reference: Octafluoroselenanthrene(16259-99-7)
    11. EPA Substance Registry System: Octafluoroselenanthrene(16259-99-7)
  • 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: 16259-99-7(Hazardous Substances Data)

16259-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16259-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,5 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16259-99:
(7*1)+(6*6)+(5*2)+(4*5)+(3*9)+(2*9)+(1*9)=127
127 % 10 = 7
So 16259-99-7 is a valid CAS Registry Number.

16259-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,6,7,8,9-octafluoroselenanthrene

1.2 Other means of identification

Product number -
Other names Selenanthrene,octafluoro

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:16259-99-7 SDS

16259-99-7Downstream Products

16259-99-7Relevant articles and documents

THE SYNTHESIS AND CRYSTAL STRUCTURE OF PERFLUOROTELLURANTHRENE, C12F8Te2

Rainville, David P.,Zingard, Ralph A.,Meyers, Edward A.

, p. 245 - 256 (1980)

The reaction of tetrafluoro-1,2-diiodobenzene with tellurium yields an oil which, on treatment with bromine yields perfluorotelluranthrene-9,9,10,10-tetrabromide.The latter is reduced by sodium sulfide to perfluorotelluranthrene.The crystal structure of perfluorotelluranthrene is reported.

THE STRUCTURE OF A TRICLINIC FORM OF OCTAFLUOROSELENANTHRENE, (C6F4)2Se2

Brown, D.S.,Mistry, T. K.,Massey, A. G.

, p. 207 - 210 (1986)

Octafluoroselenthrene exists in two different crystal forms, monoclinic and triclinic.It is shown here that the molecular structure in the triclinic modification is very similar to that found previously in monoclinic crystals.

DODECAFLUORO-5,10-o-BENZENOARSANTHRENE AND DODECAFLUORO-5,10-o-BENZENOSTIBANTHRENE

Mistry, T.K.,Massey, A.G.

, p. 45 - 47 (1981)

To clear some confusion in the literature, the "direct syntheses" of As2(C6F4)3 and of Sb2(C6F4)3 have been repeated and the identities of the compounds confirmed by analytical data and spectroscopic methods.Mixtures of As and Sb, when heated with 1,2-I2C6F4, give As2(C6F4)3, Sb2(C6F4)3 and AsSb(C6F4)3.When Sb is heated with 1,2-I2C6H4 and 1,2-I2C6F4, three compounds are formed: Sb2(C6F4)3, Sb2(C6F4)2(C6H4) and Sb(C6F4)(C6H4)2.

TRANSMETALLATION REACTIONS INVOLVING PHENYLENEMERCURIALS

Humphries, R. E.,Al-Jabar, N. A. A.,Bowen, D.,Massey, A. G.,Deacon, G. B.

, p. 59 - 68 (2007/10/02)

When heated with Group V and Group VI elements, the phenylenemercurials (C6H4Hg)3, (C6F4Hg)3 and (C6Cl4Hg)3 form heterocycles of formulae M2(C6X4)3 and M'2(C6X4)2 where M = As, Sb, Bi and M' = S, Se, Te.The compounds Te2(C6Cl4)2 and M2(C6Cl4)3 (M = As, Sb, Bi) were also obtained by heating the elements with 1,2-I2C6Cl4, which was prepared by mercuration of 1,2-H2C6Cl4 followed by iododemercuration.Octachlorothianthrene has been obtained by heating sulphur with Te2(C6Cl4)2, C6Cl6 or C6H5I, and from the reaction between 1,2-H2C6Cl4, AlCl3, and S2Cl2.

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