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230623-67-3

N,N-bis(4-n-butylphenyl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 230623-67-3 Structure

  • Basic information

    1. Product Name: N,N-bis(4-n-butylphenyl)aniline
    2. Synonyms: N,N-bis(4-n-butylphenyl)aniline
    3. CAS NO:230623-67-3
    4. Molecular Formula:
    5. Molecular Weight: 387.565
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 230623-67-3.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,N-bis(4-n-butylphenyl)aniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-bis(4-n-butylphenyl)aniline(230623-67-3)
    11. EPA Substance Registry System: N,N-bis(4-n-butylphenyl)aniline(230623-67-3)

  • 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: 230623-67-3(Hazardous Substances Data)

230623-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 230623-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,0,6,2 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 230623-67:
(8*2)+(7*3)+(6*0)+(5*6)+(4*2)+(3*3)+(2*6)+(1*7)=103
103 % 10 = 3
So 230623-67-3 is a valid CAS Registry Number.

230623-67-3Relevant articles and documents

Synthesis of functionalized organic second-order nonlinear optical chromophores for electrooptic applications

Thayumanavan,Mendez, Jeffrey,Marder, Seth R.

, p. 4289 - 4297 (1999)

The design and syntheses of functionalized second-order nonlinear optical chromophores, suitable for covalent incorporation into functionalized high-performance polymers, are described. The chromophores with hydroxy alkyl functionality have diarylamino groups as the donor moiety and a styryl thiophene moiety as the conjugated bridge. The triarylamine parts of the molecules were synthesized using palladium-catalyzed C-N bond forming reactions. The conjugated bridge was assembled using the Wittig reaction. The acceptor groups were installed in the last steps of the syntheses.

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