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1H-1,2,4-Triazol-3-amine, N-[(4-methoxyphenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5295-20-5

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5295-20-5 Usage

Structure

A derivative of 1H-1,2,4-triazole with a 4-methoxyphenylmethylene substituent

Potential applications

a. Development of pharmaceuticals or agrochemicals
b. Building block in organic synthesis for creating new compounds
c. Study of biological activities and interactions with biological systems

Fields of application

a. Medicine
b. Agriculture
c. Chemical research

Check Digit Verification of cas no

The CAS Registry Mumber 5295-20-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5295-20:
(6*5)+(5*2)+(4*9)+(3*5)+(2*2)+(1*0)=95
95 % 10 = 5
So 5295-20-5 is a valid CAS Registry Number.

5295-20-5SDS

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 1-(4-methoxyphenyl)-N-(1H-1,2,4-triazol-5-yl)methanimine

1.2 Other means of identification

Product number -
Other names 5-(4'-Methoxybenzylidene)-amino-1H-1,2,4-triazole

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:5295-20-5 SDS

5295-20-5Relevant academic research and scientific papers

HETEROCYCLIC COMPOUND AND HARMFUL-ARTHROPOD CONTROL AGENT CONTAINING SAME

-

Paragraph 0424-0425, (2020/06/15)

A compound represented by formula (I), which is highly effective in controlling harmful arthropods, an intermediate thereof and a production method thereof are described. In formula (I), A1 represents CH or a nitrogen atom; R1 repres

Structure investigations of Schiff bases derived from 3-amino-1H-1,2,4-triazole

Ko?odziej, Beata,Morawiak, Maja,Schilf, Wojciech,Kamieński, Bohdan

, p. 207 - 218 (2019/02/19)

In the present paper, twelve Schiff bases derived from 3-amino-1H-1,2,4-triazole (ATz) and various benzaldehydes, and salicylaldehydes were synthesized. The 1H, 13C, and 15N NMR data are discussed in relation to the structure of ATz and its imine products. In addition, X-ray, ATR-FTIR, and UV–Vis analytical techniques are used for structure elucidation of ATz-based Schiff bases. It was found that the starting material, 3-amino-1H-1,2,4-triazole, exists as tautomeric mixture of three forms (Graphical Abstract) in solution, whereas in the solid state (13C and 15N CPMAS data) potentially tautomeric proton is located on nitrogen atom traditionally marked as N-2 (Graphical Abstract, 2N–H structure). All investigated Schiff bases derived from salicylaldehydes exist in both phases as tautomeric equilibrium mixtures, where enol-imine forms are dominated structures. The positions of those equilibria only very slightly depend on substituents in phenol ring. Generally, the contributions of keto-amine forms in the solid state are higher comparing with DMSO solutions.

HETEROCYCLIC COMPOUND AND HARMFUL ARTHROPOD CONTROLLING AGENT CONTAINING THE SAME

-

Paragraph 0123, (2019/03/26)

PROBLEM TO BE SOLVED: To provide a compound having excellent effect for controlling harmful arthropod. SOLUTION: There is provided a compound having an excellent controlling effect against harmful arthropod, the compound being represented by the formula (

METHOD OF CONTROLLING HARMFUL ARTHROPOD USING HETEROCYCLIC COMPOUND

-

Paragraph 0230, (2019/05/30)

PROBLEM TO BE SOLVED: To provide a method of controlling a harmful arthropod. SOLUTION: A method of controlling a harmful arthropod uses a compound represented by formula (I) or an N oxide thereof. [A1 is CH or N; R1 is a halogen-sub

[4+2] Cycloaddition reaction: Synthesis and antifungal activities of 2-substituted 1,2,4-triazolo[3,2-c][1,3,5]thiadiazine-3,3-dioxides

Borthakur, Susanta K.,Boruah, Paran,Goswami, Birendra N.

, p. 1005 - 1008 (2013/09/23)

3-Benzylidineamino-1,2,4-triazole undergoes [4+2] cycloaddition reaction with sulfene resulting in good yield of [1,2,4]-triazolo[3,2-c][1,3,5]- thiadiazine-3,3-dioxide derivatives. The title compounds have been screened for their antifungal activities.

1H NMR, 13C NMR and mass spectral studies of some Schiff bases derived from 3-amino-1,2,4-triazole

Issa,Hassib,Abdelaal

experimental part, p. 902 - 910 (2010/03/30)

Heterocyclic Schiff bases derived from 3-amino-1,2,4-triazole and different substituted aromatic aldehydes are prepared and subjected to 1H NMR, 13C NMR and mass spectral analyses. 1H NMR spectra in DMSO exhibit a sharp si

Spectroscopic and Conductometric Studies on some Schiff Bases

Ayad, M. M.,Mansour, I. A.

, p. 385 - 392 (2007/10/02)

The electronic absorption spectra of some Schiff bases derived from 3-amino-1,2,4-triazole have been investigated in organic solvents of different polarities.Assignment of the absorption bands, solvent effects, and spectral structure correlations are cons

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