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CAS

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93321-17-6

1-Naphthalenemethanol, 4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93321-17-6 Structure

  • Basic information

    1. Product Name: 1-Naphthalenemethanol, 4-phenyl-
    2. Synonyms:
    3. CAS NO:93321-17-6
    4. Molecular Formula: C17H14O
    5. Molecular Weight: 234.298
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93321-17-6.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: 1-Naphthalenemethanol, 4-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Naphthalenemethanol, 4-phenyl-(93321-17-6)
    11. EPA Substance Registry System: 1-Naphthalenemethanol, 4-phenyl-(93321-17-6)

  • 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: 93321-17-6(Hazardous Substances Data)

93321-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93321-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,3,2 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93321-17:
(7*9)+(6*3)+(5*3)+(4*2)+(3*1)+(2*1)+(1*7)=116
116 % 10 = 6
So 93321-17-6 is a valid CAS Registry Number.

93321-17-6Relevant articles and documents

Pd-catalyzed allylative dearomatisation using Grignard reagents

Boldrini, Cosimo,Harutyunyan, Syuzanna R.

, p. 11807 - 11810 (2021/11/30)

Pd-catalyzed allylative dearomatisation of naphthyl halides is shown to be feasible by employing Grignard reagents. The high reactivity of the nucleophile allows for fast reactions and low catalyst loading, while a plethora of successfully substituted compounds illustrate the broad scope. Five membered heteroaromatic compounds are also demonstrated to be reactive under similar conditions.

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