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CAS

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163224-03-1

2-(selenophenylsulfonyl)cyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 163224-03-1 Structure

  • Basic information

    1. Product Name: 2-(selenophenylsulfonyl)cyclohexane
    2. Synonyms: 2-(selenophenylsulfonyl)cyclohexane
    3. CAS NO:163224-03-1
    4. Molecular Formula:
    5. Molecular Weight: 317.267
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 163224-03-1.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: 2-(selenophenylsulfonyl)cyclohexane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(selenophenylsulfonyl)cyclohexane(163224-03-1)
    11. EPA Substance Registry System: 2-(selenophenylsulfonyl)cyclohexane(163224-03-1)

  • 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: 163224-03-1(Hazardous Substances Data)

163224-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 163224-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,2,2 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 163224-03:
(8*1)+(7*6)+(6*3)+(5*2)+(4*2)+(3*4)+(2*0)+(1*3)=101
101 % 10 = 1
So 163224-03-1 is a valid CAS Registry Number.

163224-03-1Downstream Products

163224-03-1Relevant articles and documents

Phenylsulfinylselenyl Chloride (PhSO2SeCl): A New Reagent for the Formation of C-Se and N-Se Bonds. Generation and In Situ Diels-Alder Trapping of Selenonitrosoarene Intermediates (Ar-N=Se)

Bryce, Martin R.,Chesney, Antony

, p. 195 - 196 (1995)

The novel electrophilic selenium transfer reagent phenylsulfinylselenyl chloride, PhSO2SeCl, 3 has been prepared and reacted with enolisable carbonyl compounds to yield α-selenoketones and diselenides; reaction of reagent 3 with arylamines in the presence

Di(phenylsulfonyl) diselenide (PhSO2Se)2 and phenylsulfonylselenyl chloride (PhSO2SeCl) as new selenium-transfer reagents in the synthesis of functionalised diselenides and selenides

Chesney,Bryce,Cooke

, p. 1521 - 1524 (2007/10/02)

The title electrophilic selenium reagents have been used to synthesise functionalised diselenides and selenides.

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