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114329-64-5

2-(4-chloro-phenyl)-2H-naphtho[1,2-d][1,2,3]triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114329-64-5 Structure

  • Basic information

    1. Product Name: 2-(4-chloro-phenyl)-2H-naphtho[1,2-d][1,2,3]triazole
    2. Synonyms: 2-(4-chloro-phenyl)-2H-naphtho[1,2-d][1,2,3]triazole
    3. CAS NO:114329-64-5
    4. Molecular Formula:
    5. Molecular Weight: 279.728
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114329-64-5.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-(4-chloro-phenyl)-2H-naphtho[1,2-d][1,2,3]triazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-chloro-phenyl)-2H-naphtho[1,2-d][1,2,3]triazole(114329-64-5)
    11. EPA Substance Registry System: 2-(4-chloro-phenyl)-2H-naphtho[1,2-d][1,2,3]triazole(114329-64-5)

  • 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: 114329-64-5(Hazardous Substances Data)

114329-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114329-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,2 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 114329-64:
(8*1)+(7*1)+(6*4)+(5*3)+(4*2)+(3*9)+(2*6)+(1*4)=105
105 % 10 = 5
So 114329-64-5 is a valid CAS Registry Number.

114329-64-5Downstream Products

114329-64-5Relevant articles and documents

A Simple Route to 2H-Naphtho1,2,3-triazoles

Hartmann, H.,Schulze, M.,Guenther, R.

, p. 331 - 335 (2007/10/02)

1-Arylazo-2-chloro-naphthalenes 9a-9k and 2,4-diarylazo-1-chloronaphthalenes 10a-10c are transformed by the reaction with sodium azide into 2-arylsubstituted 2H-Naphtho1,2,3-triazoles 13a-13k and 14a-14c, resp., which exhibit fluorescence if they a

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