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diphenyl-di-p-tolyl-phosphonium; iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123104-36-9 Structure
  • Basic information

    1. Product Name: diphenyl-di-p-tolyl-phosphonium; iodide
    2. Synonyms: diphenyl-di-p-tolyl-phosphonium; iodide
    3. CAS NO:123104-36-9
    4. Molecular Formula:
    5. Molecular Weight: 494.355
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123104-36-9.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: diphenyl-di-p-tolyl-phosphonium; iodide(CAS DataBase Reference)
    10. NIST Chemistry Reference: diphenyl-di-p-tolyl-phosphonium; iodide(123104-36-9)
    11. EPA Substance Registry System: diphenyl-di-p-tolyl-phosphonium; iodide(123104-36-9)
  • 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: 123104-36-9(Hazardous Substances Data)

123104-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123104-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,1,0 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 123104-36:
(8*1)+(7*2)+(6*3)+(5*1)+(4*0)+(3*4)+(2*3)+(1*6)=69
69 % 10 = 9
So 123104-36-9 is a valid CAS Registry Number.

123104-36-9Downstream Products

123104-36-9Relevant articles and documents

Versatile Visible-Light-Driven Synthesis of Asymmetrical Phosphines and Phosphonium Salts

Arockiam, Percia Beatrice,Lennert, Ulrich,Graf, Christina,Rothfelder, Robin,Scott, Daniel J.,Fischer, Tillmann G.,Zeitler, Kirsten,Wolf, Robert

supporting information, p. 16374 - 16382 (2020/11/03)

Asymmetrically substituted tertiary phosphines and quaternary phosphonium salts are used extensively in applications throughout industry and academia. Despite their significance, classical methods to synthesize such compounds often demand either harsh reaction conditions, prefunctionalization of starting materials, highly sensitive organometallic reagents, or expensive transition-metal catalysts. Mild, practical methods thus remain elusive, despite being of great current interest. Herein, we describe a visible-light-driven method to form these products from secondary and primary phosphines. Using an inexpensive organic photocatalyst and blue-light irradiation, arylphosphines can be both alkylated and arylated using commercially available organohalides. In addition, the same organocatalyst can be used to transform white phosphorus (P4) directly into symmetrical aryl phosphines and phosphonium salts in a single reaction step, which has previously only been possible using precious metal catalysis.

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