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CAS

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1567382-71-1

2-(ethylamino)-3-phenylnaphthalene-1,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1567382-71-1 Structure

  • Basic information

    1. Product Name: 2-(ethylamino)-3-phenylnaphthalene-1,4-dione
    2. Synonyms: 2-(ethylamino)-3-phenylnaphthalene-1,4-dione
    3. CAS NO:1567382-71-1
    4. Molecular Formula:
    5. Molecular Weight: 277.323
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1567382-71-1.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: 2-(ethylamino)-3-phenylnaphthalene-1,4-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(ethylamino)-3-phenylnaphthalene-1,4-dione(1567382-71-1)
    11. EPA Substance Registry System: 2-(ethylamino)-3-phenylnaphthalene-1,4-dione(1567382-71-1)

  • 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: 1567382-71-1(Hazardous Substances Data)

1567382-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1567382-71-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,7,3,8 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1567382-71:
(9*1)+(8*5)+(7*6)+(6*7)+(5*3)+(4*8)+(3*2)+(2*7)+(1*1)=201
201 % 10 = 1
So 1567382-71-1 is a valid CAS Registry Number.

1567382-71-1Downstream Products

1567382-71-1Relevant articles and documents

Aryl-free radical-mediated oxidative arylation of naphthoquinones using o-iodoxybenzoic acid and phenylhydrazines and its application toward the synthesis of benzocarbazoledione

Patil, Pravin,Nimonkar, Abhay,Akamanchi, Krishnacharya G.

, p. 2331 - 2336 (2014)

Oxidative arylation of naphthoquinones has been developed through combination of o-iodoxybenzoic acid with arylhydrazines under mild conditions at open atmosphere. Arylated naphthoquinones with different electronic properties were obtained in moderate to good yields. The postulated radical mediated mechanism is supported by radical trapping experiments. Developed protocol for direct arylation of naphthoquinones has been extended toward short, high yielding, and an effective synthesis of antitumor-antibiotic precursor such as benzocarbazoledione.

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