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(1E)-1-benzyl-3-phenyltriaz-1-ene, also known as Benzyl phenyl triazole, is a chemical compound with the molecular formula C14H12N2. It belongs to the class of organic compounds known as triazoles, which are a group of heterocyclic compounds containing a five-membered ring of two carbon atoms and three nitrogen atoms. This particular compound is a triazole derivative with a benzyl group attached to one end and a phenyl group attached to the other end of the triazole core. It is commonly used in organic synthesis and medicinal chemistry, and has various applications in the development of pharmaceutical drugs and agrochemicals. Benzyl phenyl triazole exhibits potential biological activities, including antifungal and antibacterial properties, and has been a subject of research in the fields of drug design and discovery.

17683-10-2

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17683-10-2 Usage

Uses

Used in Pharmaceutical Industry:
(1E)-1-benzyl-3-phenyltriaz-1-ene is used as a building block in the synthesis of pharmaceutical drugs for its versatile chemical properties and potential biological activities.
Used in Agrochemical Industry:
(1E)-1-benzyl-3-phenyltriaz-1-ene is used as a precursor in the development of agrochemicals for its antifungal and antibacterial properties, contributing to the protection and enhancement of crop yields.
Used in Drug Design and Discovery:
(1E)-1-benzyl-3-phenyltriaz-1-ene is used as a research compound in drug design and discovery for its potential to be modified and optimized for various therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 17683-10-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,8 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17683-10:
(7*1)+(6*7)+(5*6)+(4*8)+(3*3)+(2*1)+(1*0)=122
122 % 10 = 2
So 17683-10-2 is a valid CAS Registry Number.

17683-10-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(benzyldiazenyl)aniline

1.2 Other means of identification

Product number -
Other names N-benzyl-N'-phenyl-triazene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17683-10-2 SDS

17683-10-2Relevant academic research and scientific papers

Pathways for the Decomposition of Alkylaryltriazenes in Aqueous Solution

Jones, Caroline C.,Kelly, Migel A.,Sinnott, Michael L.,Smith, Paul J.,Tzotzos, George T.

, p. 1655 - 1664 (2007/10/02)

Primary alkylaryltriazenes give solvent-equilibrated alkenediazonium ions and anilines in aqueous solution at 25 deg C by two processes.The first, an A-SE2(N) reaction, involves immobilisation of a molecule of catalysing acid, and a transition state in which the proton is essentially completely transferred and little breakage of the N-N bond has occurred.The structure of this transition state varies with the strength of the catalysing acid and the pKa of the liberated aniline in a way interpretable in terms of a More O'Ferrall-Jencks diagram.The second process is the departure of aniline anion without acid assistance.The first process is governed by positive, the second by negative, βlg values.

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