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n-butyltriphenylphoshonium tosylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 106503-53-1 Structure
  • Basic information

    1. Product Name: n-butyltriphenylphoshonium tosylate
    2. Synonyms: n-butyltriphenylphoshonium tosylate
    3. CAS NO:106503-53-1
    4. Molecular Formula:
    5. Molecular Weight: 490.603
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 106503-53-1.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: n-butyltriphenylphoshonium tosylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: n-butyltriphenylphoshonium tosylate(106503-53-1)
    11. EPA Substance Registry System: n-butyltriphenylphoshonium tosylate(106503-53-1)
  • 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: 106503-53-1(Hazardous Substances Data)

106503-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106503-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,5,0 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106503-53:
(8*1)+(7*0)+(6*6)+(5*5)+(4*0)+(3*3)+(2*5)+(1*3)=91
91 % 10 = 1
So 106503-53-1 is a valid CAS Registry Number.

106503-53-1Downstream Products

106503-53-1Relevant articles and documents

Ionic liquids: Synthesis and characterisation of triphenylphosphonium tosylates

Bonnet, Ludovic G.,Kariuki, Benson M.

, p. 437 - 446 (2006)

Ionic liquids are currently attracting considerable interest from chemists, partly due to their potential as "green" alternatives to volatile molecular organic solvents. Phosphonium ionic liquids have received much less attention than ammonium salts in th

Quaternary phosphonium salt flame retardant and synthesis method and application thereof

-

Paragraph 0170-0174, (2020/06/20)

The invention provides a quaternary phosphonium salt flame retardant and a synthesis method and application thereof, and the method comprises the following steps: by taking an acidic compound, ortho-formic acid trisubstituted ester and an organic phosphine compound III or IV as raw materials, carrying out a one-step reaction process to prepare the quaternary phosphonium salt flame retardant I or II. The flame retardant disclosed by the invention has good thermal stability and has an excellent flame-retardant effect when being applied to various polymers. The method is simple and convenient insynthesis operation, low in raw material price, mild in synthesis condition and high in yield. According to the synthesis method, introduction of halogen ions is avoided, and dozens of anions are successfully introduced. By adding a small amount of the flame retardant, the obtained PC flame-retardant composite material UL-94 can reach the V-0 grade.

Clean catalysis with ionic solvents - Phosphonium tosylates for hydroformylation

Karodia, Nazira,Guise, Steven,Newlands, Craig,Andersen, Jo-Ann

, p. 2341 - 2342 (2007/10/03)

High-melting phosphonium tosylates are synthesised and applied for the first time as solvents in catalytic hydroformylation reactions; variation in the substituents attached to phosphorus can lead to markedly different results; the catalyst systems are non-corrosive, easily manipulated and can readily be recovered and reused.

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