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134654-78-7

Phosphorin, 2-(diphenylphosphino)-4,5-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134654-78-7 Structure

  • Basic information

    1. Product Name: Phosphorin, 2-(diphenylphosphino)-4,5-dimethyl-
    2. Synonyms:
    3. CAS NO:134654-78-7
    4. Molecular Formula: C19H18P2
    5. Molecular Weight: 308.299
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134654-78-7.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: Phosphorin, 2-(diphenylphosphino)-4,5-dimethyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphorin, 2-(diphenylphosphino)-4,5-dimethyl-(134654-78-7)
    11. EPA Substance Registry System: Phosphorin, 2-(diphenylphosphino)-4,5-dimethyl-(134654-78-7)

  • 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: 134654-78-7(Hazardous Substances Data)

134654-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134654-78-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,6,5 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 134654-78:
(8*1)+(7*3)+(6*4)+(5*6)+(4*5)+(3*4)+(2*7)+(1*8)=137
137 % 10 = 7
So 134654-78-7 is a valid CAS Registry Number.

134654-78-7Relevant articles and documents

Palladium(0)-catalyzed functionalization of bromophosphinines

Le Floch, Pascal,Carmichael, Duncan,Ricard, Louis,Mathey, Fran?ois

, p. 10665 - 10670 (1993)

[PdL2]-catalyzed (L = triphenyl- or trifurylphosphine) cross-coupling of 2,4,6-tribromo- or 2,6-dibromophosphinines with R-SnMe3 derivatives yields the corresponding 2,6-di-R-phosphinines, where R = 2-furyl, 2-thienyl, 2-N-methylpyrrolyl, or C≡C-Ph. When R is 2-pyridyl, only the monosubstituted phosphinine is obtained. A similar cross-coupling reaction between 2,4,6-tribromo- or 2-bromophosphinines and (trimethylsilyl)diphenylphosphine gives either 2,6-bis(diphenylphosphino)- or 2-(diphenylphosphino)phosphinines according to the starting materials. In the case of 2,4,6-tribromophosphinines, the ortho selectivity of the functionalizations probably reflects an initial coordination of [PdL2] to the phosphinine phosphorus.

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