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893-39-0

(1E)-1,3-bis(2,5-dichlorophenyl)triaz-1-ene, with the molecular formula C15H8Cl4N2, is a chemical compound belonging to the class of organic compounds known as triazoles. This class features five-membered heterocyclic compounds that contain a triazole ring, which consists of two carbon atoms and three nitrogen atoms. Additionally, (1E)-1,3-bis(2,5-dichlorophenyl)triaz-1-ene is a type of triene, characterized by a conjugated system of three double bonds. Its unique chemical structure renders it a valuable building block in the synthesis of various organic compounds, particularly in the development of pharmaceuticals, agrochemicals, and other biologically active substances. However, due to potential health and environmental hazards, it is crucial to handle (1E)-1,3-bis(2,5-dichlorophenyl)triaz-1-ene with care.

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  • 893-39-0 Structure

  • Basic information

    1. Product Name: (1E)-1,3-bis(2,5-dichlorophenyl)triaz-1-ene
    2. Synonyms:
    3. CAS NO:893-39-0
    4. Molecular Formula: C12H7Cl4N3
    5. Molecular Weight: 335.0161
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 893-39-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 425.8°C at 760 mmHg
    3. Flash Point: 211.3°C
    4. Appearance: N/A
    5. Density: 1.52g/cm3
    6. Vapor Pressure: 1.86E-07mmHg at 25°C
    7. Refractive Index: 1.65
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (1E)-1,3-bis(2,5-dichlorophenyl)triaz-1-ene(CAS DataBase Reference)
    11. NIST Chemistry Reference: (1E)-1,3-bis(2,5-dichlorophenyl)triaz-1-ene(893-39-0)
    12. EPA Substance Registry System: (1E)-1,3-bis(2,5-dichlorophenyl)triaz-1-ene(893-39-0)

  • 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: 893-39-0(Hazardous Substances Data)

893-39-0 Usage

Uses

Used in Pharmaceutical Industry:
(1E)-1,3-bis(2,5-dichlorophenyl)triaz-1-ene is used as a building block for the synthesis of pharmaceuticals due to its unique triazole ring and conjugated triene system. Its chemical properties make it a promising candidate for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, (1E)-1,3-bis(2,5-dichlorophenyl)triaz-1-ene is utilized as a precursor in the synthesis of various agrochemicals. Its structure contributes to the creation of compounds that can be used in pest control and crop protection, enhancing agricultural productivity.
Used in Laboratory Research:
(1E)-1,3-bis(2,5-dichlorophenyl)triaz-1-ene is also used in laboratory research as a key component in the synthesis of a wide range of organic compounds. Its versatility in chemical reactions allows researchers to explore its potential applications in various fields, including materials science and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 893-39-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 893-39:
(5*8)+(4*9)+(3*3)+(2*3)+(1*9)=100
100 % 10 = 0
So 893-39-0 is a valid CAS Registry Number.

893-39-0Relevant articles and documents

Synthesis and biological evaluation of 4-nitro-substituted 1,3-diaryltriazenes as a novel class of potent antitumor agents

?imbora-Zovko, Tamara,Brozovic, Anamaria,Piantanida, Ivo,Fritz, Gerhard,Virag, Andrej,Ali?, Branko,Majce, Vita,Ko?evar, Marijan,Polanc, Slovenko,Osmak, Maja

experimental part, p. 2971 - 2983 (2011/07/09)

We describe the synthesis and biological activity of a new class of 1,3-diaryltriazenes, namely 4-nitro-substituted 1,3-diaryltriazenes. Structure-activity relationship analysis reveals that 1,3-diaryltriazenes can be modified from inactive to highly cyto

A ligand-free copper (1) catalysed intramolecular N-arylation of diazoaminobenzenes in PEG-water: An expeditious protocol towards regiospecific 1-aryl benzotriazoles

Mukhopadhyay, Chhanda,Tapaswi, Pradip Kumar,Butcher, Ray J.

supporting information; experimental part, p. 4720 - 4729 (2010/11/17)

An efficient and highly versatile method for the synthesis of diverse regiospecific 1-arylbenzotriazoles being important medicinal scaffolds, by the copper (1) catalysed intramolecular N-arylation of diazoaminobenzenes of 2-haloaryldiazonium salts in PEG-water has been developed. A very simple reaction protocol, large number of substrate affordability and excellent yields are the main features of this methodology.

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