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688047-86-1

W(CO)5PCH2C6H5C4H2(CH3)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 688047-86-1 Structure

  • Basic information

    1. Product Name: W(CO)5PCH2C6H5C4H2(CH3)2
    2. Synonyms:
    3. CAS NO:688047-86-1
    4. Molecular Formula:
    5. Molecular Weight: 526.138
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 688047-86-1.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: W(CO)5PCH2C6H5C4H2(CH3)2(CAS DataBase Reference)
    10. NIST Chemistry Reference: W(CO)5PCH2C6H5C4H2(CH3)2(688047-86-1)
    11. EPA Substance Registry System: W(CO)5PCH2C6H5C4H2(CH3)2(688047-86-1)

  • 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: 688047-86-1(Hazardous Substances Data)

688047-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 688047-86-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,8,0,4 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 688047-86:
(8*6)+(7*8)+(6*8)+(5*0)+(4*4)+(3*7)+(2*8)+(1*6)=211
211 % 10 = 1
So 688047-86-1 is a valid CAS Registry Number.

688047-86-1Downstream Products

688047-86-1Relevant articles and documents

Using monovalent phosphorus compounds to form P-C bonds

Ng, Yong Xiang,Mathey, Francois

, p. 14140 - 14142 (2013)

User friendly P-C: Electrophilic terminal phosphinidene complexes [RP-W(CO)5] react with Ar-B(OH)2 to give the corresponding secondary phosphine complexes [{R(Ar)PH}W(CO)5]. This method enables the formation of P-C bonds through the combination of a wide array of heterocyclic and aryl boronic acids with various electrophilic phosphinidene complexes. The final products incorporate a P-H bond that can be used for further transformations. Copyright

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