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10148-02-4

1-(4'-chlorobenzeneazo)-2-amino-naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10148-02-4 Structure

  • Basic information

    1. Product Name: 1-(4'-chlorobenzeneazo)-2-amino-naphthalene
    2. Synonyms: 1-(4'-chlorobenzeneazo)-2-amino-naphthalene
    3. CAS NO:10148-02-4
    4. Molecular Formula:
    5. Molecular Weight: 281.744
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10148-02-4.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-(4'-chlorobenzeneazo)-2-amino-naphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4'-chlorobenzeneazo)-2-amino-naphthalene(10148-02-4)
    11. EPA Substance Registry System: 1-(4'-chlorobenzeneazo)-2-amino-naphthalene(10148-02-4)

  • 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: 10148-02-4(Hazardous Substances Data)

10148-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10148-02-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,4 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10148-02:
(7*1)+(6*0)+(5*1)+(4*4)+(3*8)+(2*0)+(1*2)=54
54 % 10 = 4
So 10148-02-4 is a valid CAS Registry Number.

10148-02-4Relevant articles and documents

A simple route to 2-aryl-substituted naphtho[2,1-e][1,2,4]triazinium and naphtho[2,1-e][1,2,3,4]tetrazinium salts from 1-arylazo-substituted 2-naphthylamines

Yu, Xiuling,Metz, Peter,Hartmann, Horst

, p. 431 - 435 (2018)

1-Arylazo-substituted 2-naphthylamines, which are easily obtainable by the coupling of arene diazonium salts with 2-aminonaphthalene-sulfonic acid, can be transformed by reaction with reactive carboxylic acid derivatives or nitrosation reagents into novel 2-aryl-substituted naphtho[2,1-e][1,2,4]triazinium and naphtho[2,1-e][1,2,3,4]tetrazinium salts, respectively.

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