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CAS

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130056-46-1

4-(4-pentylphenyl)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130056-46-1 Structure

  • Basic information

    1. Product Name: 4-(4-pentylphenyl)pyridine
    2. Synonyms: 4-(4-pentylphenyl)pyridine
    3. CAS NO:130056-46-1
    4. Molecular Formula:
    5. Molecular Weight: 225.334
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130056-46-1.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: 4-(4-pentylphenyl)pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-pentylphenyl)pyridine(130056-46-1)
    11. EPA Substance Registry System: 4-(4-pentylphenyl)pyridine(130056-46-1)

  • 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: 130056-46-1(Hazardous Substances Data)

130056-46-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130056-46-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,0,5 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130056-46:
(8*1)+(7*3)+(6*0)+(5*0)+(4*5)+(3*6)+(2*4)+(1*6)=81
81 % 10 = 1
So 130056-46-1 is a valid CAS Registry Number.

130056-46-1Downstream Products

130056-46-1Relevant articles and documents

C-F activation for C(sp2)-C(sp3) cross-coupling by a secondary phosphine oxide (SPO)-nickel complex

Müller, Valentin,Ghorai, Debasish,Capdevila, Lorena,Messinis, Antonis M.,Ribas, Xavi,Ackermann, Lutz

, p. 7034 - 7040 (2020)

A secondary phosphine oxide (SPO)-nickel catalyst allowed the activation of otherwise inert C-F bonds of unactivated arenes in terms of challenging couplings with primary and secondary alkyl Grignard reagents. The C-F activation is characterized by mild reaction conditions and high levels of branched selectivity. Electron-rich and electron-deficient arenes were suitable electrophiles for this transformation. In addition, this strategy also proved suitable to heterocycles and for the activation of C-O bonds under slightly modified conditions.

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