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N-[4-(dimethylamino)benzylidene]-1H-1,2,4-triazol-5-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38248-52-1

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38248-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38248-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,4 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38248-52:
(7*3)+(6*8)+(5*2)+(4*4)+(3*8)+(2*5)+(1*2)=131
131 % 10 = 1
So 38248-52-1 is a valid CAS Registry Number.

38248-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-4-[(E)-1H-1,2,4-triazol-5-yliminomethyl]aniline

1.2 Other means of identification

Product number -
Other names Apicyclina

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:38248-52-1 SDS

38248-52-1Relevant academic research and scientific papers

Antiglycation activity of triazole schiff’s bases against fructose-mediated glycation: In vitro and in silico study

Choudhary, Muhammad I.,Imad, Rehan,Khan, Khalid M.,Naqeeb, Uzma,Shaikh, Muniza,Siddiqui, Salman,Subzwari, Fakiha,Zafar, Humaira

, p. 575 - 591 (2020/06/21)

Background: Advanced glycation end products (AGEs) are known to be involved in the pathophysiology of diabetic complications, neurodegenerative diseases, and aging. Preventing the formation of AGEs can be helpful in the management of these diseases. Objec

Synthesis, β-Glucuronidase Inhibition, and Molecular Docking Studies of 1,2,4-Triazole Hydrazones

Jamil, Waqas,Kumari, Darshana,Taha, Muhammad,Khan, Muhammad Naseem,Baharudin, Mohd Syukri,Ali, Muhammad,Kanwal,Lashari, Muhammad Saleem,Khan, Khalid Muhammad

, p. 2441 - 2454 (2018/09/13)

A series of 1,2,4-triazole hydrazones 1–25 has been synthesized and characterized using different spectroscopic techniques including FT-IR, 1H-NMR, and ESI MS spectrometry. The synthetic derivatives were evaluated for their β-glucuronidase enzy

Synthesis of triazole Schiff bases: Novel inhibitors of nucleotide pyrophosphatase/phosphodiesterase-1

Khan, Khalid Mohammed,Siddiqui, Salman,Saleem, Muhammad,Taha, Muhammad,Saad, Syed Muhammad,Perveen, Shahnaz,Choudhary, M. Iqbal

supporting information, p. 6509 - 6514 (2015/02/19)

A series of Schiff base triazoles 1-25 was synthesized and evaluated for their nucleotide pyrophosphatase/phosphodiesterase-1 inhibitory activities. Among twenty-five compounds, three compounds 10 (IC50 = 132.20 ± 2.89 μM), 13 (IC50

[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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