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N-PHENYL-1H-1,2,4-TRIAZOL-5-AMINE, also known as 5-Amino-1-phenyl-1H-1,2,4-triazole, is a chemical compound characterized by the molecular formula C9H8N4. It presents as a white to light beige powder and is widely recognized for its role as an intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. This versatile intermediate is instrumental in the creation of triazoles and other nitrogen-containing compounds, contributing to the development of a broad spectrum of applications.

2433-53-6

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2433-53-6 Usage

Uses

Used in Pharmaceutical Industry:
N-PHENYL-1H-1,2,4-TRIAZOL-5-AMINE is used as a chemical intermediate for the synthesis of pharmaceuticals. It plays a crucial role in the development of new drugs, given its ability to form triazole-based compounds with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, N-PHENYL-1H-1,2,4-TRIAZOL-5-AMINE is utilized as a precursor in the production of agrochemicals. Its involvement in the synthesis of various compounds makes it a valuable asset in creating products that can protect crops and enhance agricultural yields.
Used in Organic Chemistry Research:
N-PHENYL-1H-1,2,4-TRIAZOL-5-AMINE is also used as a building block in organic chemistry for the synthesis of triazoles and other nitrogen-containing heterocycles. These compounds are essential in various chemical reactions and can lead to the discovery of new materials and applications.
Safety Considerations:
It is important to handle N-PHENYL-1H-1,2,4-TRIAZOL-5-AMINE with care due to its potential toxic effects if ingested or inhaled. Adequate safety measures, including the use of personal protective equipment and proper disposal methods, should be adopted in laboratory and industrial settings to mitigate risks associated with N-PHENYL-1H-1,2,4-TRIAZOL-5-AMINE.

Check Digit Verification of cas no

The CAS Registry Mumber 2433-53-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2433-53:
(6*2)+(5*4)+(4*3)+(3*3)+(2*5)+(1*3)=66
66 % 10 = 6
So 2433-53-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N4/c1-2-4-7(5-3-1)11-8-9-6-10-12-8/h1-6H,(H2,9,10,11,12)

2433-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenyl-1H-1,2,4-triazol-5-amine

1.2 Other means of identification

Product number -
Other names 3-Anilino-1,2,4-triazol

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:2433-53-6 SDS

2433-53-6Relevant academic research and scientific papers

A novel and convenient synthesis of 3-amino-2H-1,2,4-triazoles from isoselenocyanates and hydrazine hydrate

Li, Xue,Peng, Zhixiang,Zhang, Yuanyuan,Wang, Jiangwei,Gan, Bin,Xie, Yuanyuan

, p. 255 - 259 (2018/06/29)

A novel and convenient one-pot synthesis of 3-amino-2H-1,2,4-triazoles from two molecules of isoselenocyanates and hydrazine hydrate via cyclodeselenisation was developed. Various 3-amino-2H-1,2,4-triazoles were obtained in moderate to good yields (33-45%

Cycloaddition of synthetic equivalent of nonstabilized aminonitrile ylides: A new route to amino-substituted aΔ2-imidazolines and Δ3-1,2,4-triazolines

Tsuge, Otohiko,Hatta, Taizo,Tashiro, Hideki,Maeda, Hironori

, p. 243 - 248 (2007/10/03)

The N-unsubstituted nonstabilized azomethine ylides generated from the desilylation of N-[(trimethylsilyl)methyl]iminium triflates undergo successful cycloaddition to strongly polarized sulfonylimines and diethyl azodicarboxylate to produce the corresponding Δ2-imidazolines and Δ3-1,2,4-triazolines together with the initial cycloadducts. The initial cycloadducts are converted to the corresponding aminonitrile ylide cycloadducts. Thus the present process provides a new route to amino-substituted Δ2-imidazolines and Δ3-1,2,4-triazolines that are otherwise relatively inaccessible.

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