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541520-05-2

N-pentafluorophenylnaphthalene-1-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 541520-05-2 Structure

  • Basic information

    1. Product Name: N-pentafluorophenylnaphthalene-1-carboxamide
    2. Synonyms: N-pentafluorophenylnaphthalene-1-carboxamide
    3. CAS NO:541520-05-2
    4. Molecular Formula:
    5. Molecular Weight: 337.249
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 541520-05-2.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-pentafluorophenylnaphthalene-1-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-pentafluorophenylnaphthalene-1-carboxamide(541520-05-2)
    11. EPA Substance Registry System: N-pentafluorophenylnaphthalene-1-carboxamide(541520-05-2)

  • 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: 541520-05-2(Hazardous Substances Data)

541520-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 541520-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,1,5,2 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 541520-05:
(8*5)+(7*4)+(6*1)+(5*5)+(4*2)+(3*0)+(2*0)+(1*5)=112
112 % 10 = 2
So 541520-05-2 is a valid CAS Registry Number.

541520-05-2Downstream Products

541520-05-2Relevant articles and documents

Ligand-Promoted RhIII-Catalyzed Thiolation of Benzamides with a Broad Disulfide Scope

Kang, Yan-Shang,Zhang, Ping,Li, Min-Yan,Chen, You-Ke,Xu, Hua-Jin,Zhao, Jing,Sun, Wei-Yin,Yu, Jin-Quan,Lu, Yi

, p. 9099 - 9103 (2019)

A ligand-promoted RhIII-catalyzed C(sp2)?H activation/thiolation of benzamides has been developed. Using bidentate mono-N-protected amino acid ligands led to the first example of RhIII-catalyzed aryl thiolation reactions directed by weakly coordinating directing amide groups. The reaction tolerates a broad range of amides and disulfide reagents.

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