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Dibenzoselenophene, 5,5-dichloro-5,5-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 565454-20-8 Structure
  • Basic information

    1. Product Name: Dibenzoselenophene, 5,5-dichloro-5,5-dihydro-
    2. Synonyms:
    3. CAS NO:565454-20-8
    4. Molecular Formula: C12H8Cl2Se
    5. Molecular Weight: 302.062
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 565454-20-8.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: Dibenzoselenophene, 5,5-dichloro-5,5-dihydro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Dibenzoselenophene, 5,5-dichloro-5,5-dihydro-(565454-20-8)
    11. EPA Substance Registry System: Dibenzoselenophene, 5,5-dichloro-5,5-dihydro-(565454-20-8)
  • 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: 565454-20-8(Hazardous Substances Data)

565454-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 565454-20-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,5,4,5 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 565454-20:
(8*5)+(7*6)+(6*5)+(5*4)+(4*5)+(3*4)+(2*2)+(1*0)=168
168 % 10 = 8
So 565454-20-8 is a valid CAS Registry Number.

565454-20-8Downstream Products

565454-20-8Relevant articles and documents

Halogenation of dibenzoselenophene and dibenzo[1,2]diselenine

Klapoetke, Thomas M.,Krumm, Burkhard,Scherr, Matthias

, p. 1955 - 1961 (2010)

The syntheses of the selenium containing heterocycles di-benzoselenophene (1 ≡ biphenSe) and dibenzo[1,2]diselenine (2 ≡ biphenSe2) were optimized. The halogenation reactions of 1 and 2 with XeF2, SO2Cl2, Br2 and I2 were performed and the corresponding products characterized. In the case of 1, the selenium(IV) dihalogenides, biphenSeF2 (3), biphenSeCl2 (4), biphenSeBr2 (5), and the adduct biphenSe·I2 (6), were isolated and identified. The extremely sensitive selenium(IV) difluoride 3 slowly formed significant amounts of an adduct with HF of the corresponding selenium(IV) oxide biphen-SeO·HF (3a) upon storage in glass vessels at low temperatures. In the case of 2, the selenium(IV) trihalogenides, biphen(SeHal3)2 (Hal = F, Cl, Br), were found to be extremely labile (Hal = F) or not detectable (Hal = Cl, Br). Instead, as decomposition products, the selenium chloride species Se2Cl 2, SeCl4 and 1 were detected. In the case of Hal = I, the stable adduct biphenSe2·I2 (7) was isolated. In addition to characterization by multinuclear NMR spectroscopy, several molecular structures of biphen-selenium substituted halogenides were determined.

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