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<(5-Cyan-1,1-dioxobenzothien-2-yl)methyl>triphenylphosphoniumbromid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105191-50-2

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  • 105191-50-2 Structure
  • Basic information

    1. Product Name: <(5-Cyan-1,1-dioxobenzothien-2-yl)methyl>triphenylphosphoniumbromid
    2. Synonyms:
    3. CAS NO:105191-50-2
    4. Molecular Formula:
    5. Molecular Weight: 546.424
    6. EINECS: N/A
    7. Product Categories: N/A
  • 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: <(5-Cyan-1,1-dioxobenzothien-2-yl)methyl>triphenylphosphoniumbromid(CAS DataBase Reference)
    10. NIST Chemistry Reference: <(5-Cyan-1,1-dioxobenzothien-2-yl)methyl>triphenylphosphoniumbromid(105191-50-2)
    11. EPA Substance Registry System: <(5-Cyan-1,1-dioxobenzothien-2-yl)methyl>triphenylphosphoniumbromid(105191-50-2)
  • 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: 105191-50-2(Hazardous Substances Data)

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105191-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105191-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,1,9 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 105191-50:
(8*1)+(7*0)+(6*5)+(5*1)+(4*9)+(3*1)+(2*5)+(1*0)=92
92 % 10 = 2
So 105191-50-2 is a valid CAS Registry Number.

105191-50-2Downstream Products

105191-50-2Relevant academic research and scientific papers

Synthesis of Antileukemic Indolylvinyl-1-benzofurans and -benzothiophenes

Dann, Otto,Char, Helmut,Fleischmann, Paul,Fricke, Helmut

, p. 438 - 455 (2007/10/02)

2--1-benzofuran and -benzothiophene compounds 6-13 and 18-22 with terminal amidinium or imidazolinium groups were synthesized; in their antileukemic activity in mice they surpass the isosteric 2,2'-vinylenebis(1-benzofuran) and -(benzo-thiophene) compounds.

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