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1395898-02-8

AuPh2(2-(p-tolyl)pyridine) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1395898-02-8 Structure

  • Basic information

    1. Product Name: AuPh2(2-(p-tolyl)pyridine)
    2. Synonyms: AuPh2(2-(p-tolyl)pyridine)
    3. CAS NO:1395898-02-8
    4. Molecular Formula:
    5. Molecular Weight: 519.396
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1395898-02-8.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: AuPh2(2-(p-tolyl)pyridine)(CAS DataBase Reference)
    10. NIST Chemistry Reference: AuPh2(2-(p-tolyl)pyridine)(1395898-02-8)
    11. EPA Substance Registry System: AuPh2(2-(p-tolyl)pyridine)(1395898-02-8)

  • 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: 1395898-02-8(Hazardous Substances Data)

1395898-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1395898-02-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,5,8,9 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1395898-02:
(9*1)+(8*3)+(7*9)+(6*5)+(5*8)+(4*9)+(3*8)+(2*0)+(1*2)=228
228 % 10 = 8
So 1395898-02-8 is a valid CAS Registry Number.

1395898-02-8Downstream Products

1395898-02-8Relevant articles and documents

Suzuki-Miyaura coupling of arylboronic acids to gold(III)

Maity, Ayan,Sulicz, Amanda N.,Deligonul, Nihal,Zeller, Matthias,Hunter, Allen D.,Gray, Thomas G.

, p. 981 - 986 (2015)

Gold(III) is prominent in catalysis, but its organometallic chemistry continues to be restricted by synthesis. Metal-carbon bond formation often relies on organometallic complexes of electropositive elements, including lithium and magnesium. The redox potential of gold(III) interferes with reactions of these classic reagents. Resort to toxic metals is common, including reagents based on mercury and thallium. We report that the palladium-catalyzed Suzuki-Miyaura coupling of arylboronic acids extends to cyclometalated gold(III) chlorides. Both monoarylation and diarylation are achieved. We propose a mechanism where oxidative addition to palladium with rearrangement at gold(III) fixes the stereochemistry of monoarylated intermediates. Singly arylated species form as thermodynamic isomers. These entities then go on to form diarylated complexes. Reactions proceed at room temperature, and the products are stable to air, moisture, and chromatography.

Versatile methods for preparation of new cyclometalated gold(III) complexes

Langseth, Eirin,Goerbitz, Carl Henrik,Heyn, Richard H.,Tilset, Mats

, p. 6567 - 6571 (2012/10/30)

Versatile methods for the high-yield syntheses of new cyclometalated gold(III) complexes are described. Mono- or dialkylated or arylated gold(III) complexes are selectively obtained from reaction of Au(OCOCF3) 2(tpy) (tpy = 2-(p-toly

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