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153908-42-0

iodo(phenylseleno)methane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 153908-42-0 Structure

  • Basic information

    1. Product Name: iodo(phenylseleno)methane
    2. Synonyms: iodo(phenylseleno)methane
    3. CAS NO:153908-42-0
    4. Molecular Formula:
    5. Molecular Weight: 296.997
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153908-42-0.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: iodo(phenylseleno)methane(CAS DataBase Reference)
    10. NIST Chemistry Reference: iodo(phenylseleno)methane(153908-42-0)
    11. EPA Substance Registry System: iodo(phenylseleno)methane(153908-42-0)

  • 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: 153908-42-0(Hazardous Substances Data)

153908-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153908-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,9,0 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 153908-42:
(8*1)+(7*5)+(6*3)+(5*9)+(4*0)+(3*8)+(2*4)+(1*2)=140
140 % 10 = 0
So 153908-42-0 is a valid CAS Registry Number.

153908-42-0Relevant articles and documents

Facile C-Se and C-S Bond Cleavages in Diorganyl Selenides and Sulfides by Iodine

Nakanishi, Waro

, p. 2121 - 2122 (1993)

The C-Se and C-S bonds in ArSeCH2SeAr, PhCH2SeCH2SeCH2Ph, (p-t-Bu-C6H4SeCH2)2, 1,8-(MeSe)2C10H6, PhCH2SeMe, PhSCH2SPh, and PhCH2SCH2SCH2Ph are easily cleaved by iodine, while those of PhSe(CH2)3SePh, 1-MeSeC10H7, PhSeCH2I, and PhCH2SMe are not.The driving force of the reaction is also discussed.

Preparation of polycyclic systems by sequential 5-exo-digonal radical cyclization, 1,5-hydrogen transfer from silicon, and 5-endo-trigonal cyclization

Clive,Yang,Macdonald,Wang,Cantin

, p. 1966 - 1983 (2007/10/03)

Radicals of type 1 undergo 5-exo diagonal cyclization, and the resulting vinyl radical abstracts hydrogen from silicon to afford a silicon-centered radical. This radical closes in a 5-endo trigonal manner to generate radicals of type 4, which are reduced

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