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1363650-08-1

α-(2-methoxynaphthyl)-2-naphthylacetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1363650-08-1 Structure

  • Basic information

    1. Product Name: α-(2-methoxynaphthyl)-2-naphthylacetonitrile
    2. Synonyms: α-(2-methoxynaphthyl)-2-naphthylacetonitrile
    3. CAS NO:1363650-08-1
    4. Molecular Formula:
    5. Molecular Weight: 323.394
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1363650-08-1.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: α-(2-methoxynaphthyl)-2-naphthylacetonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: α-(2-methoxynaphthyl)-2-naphthylacetonitrile(1363650-08-1)
    11. EPA Substance Registry System: α-(2-methoxynaphthyl)-2-naphthylacetonitrile(1363650-08-1)

  • 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: 1363650-08-1(Hazardous Substances Data)

1363650-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1363650-08-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,6,5 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1363650-08:
(9*1)+(8*3)+(7*6)+(6*3)+(5*6)+(4*5)+(3*0)+(2*0)+(1*8)=151
151 % 10 = 1
So 1363650-08-1 is a valid CAS Registry Number.

1363650-08-1Downstream Products

1363650-08-1Relevant articles and documents

Synthesis of α,α-diaryl nitriles by radical nucleophilic substitution

Tempesti, Tomas C.,Pierini, Adriana B.,Baumgartner, Maria T.

, p. 597 - 602 (2012/04/18)

The present study shows that the anion of 2-naphthylacetonitrile is substituted selectively at its Cα by aromatic halides, through a radical nucleophilic substitution mechanism, to give the corresponding α,α-diaryl nitriles in good yields. The regioselectivity of this ambident nucleophile changes with the steric hindrance at the radical centre from the aromatic substrate. The selectivity observed was investigated through a computational model of the key reaction step. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2012.

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