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1,3,4-Thiadiazol-2-amine, N-[(4-methoxyphenyl)methylene]-5-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6578-89-8

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6578-89-8 Usage

Molecular structure

Contains a thiadiazole ring, an amine group, a phenyl group, and a methoxyphenyl group.

Functional groups

Thiadiazole ring, amine group, phenyl group, and methoxyphenyl group.

Potential applications

Pharmaceutical industry, specifically in the development of drugs targeting specific biological pathways or enzymes.

Versatility

Unique structure and combination of functional groups make it a versatile building block for the synthesis of novel compounds with potential therapeutic properties.

Research and exploration

Further research and exploration of this chemical's properties and potential uses are warranted to fully understand its capabilities.

Check Digit Verification of cas no

The CAS Registry Mumber 6578-89-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6578-89:
(6*6)+(5*5)+(4*7)+(3*8)+(2*8)+(1*9)=138
138 % 10 = 8
So 6578-89-8 is a valid CAS Registry Number.

6578-89-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methoxyphenyl)-N-(5-phenyl-1,3,4-thiadiazol-2-yl)methanimine

1.2 Other means of identification

Product number -
Other names (4-methoxy-benzylidene)-(5-phenyl-[1,3,4]thiadiazol-2-yl)-amine

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:6578-89-8 SDS

6578-89-8Relevant academic research and scientific papers

Synthesis, Characterization and Biological Evaluation of Some Novel Azo-Imine Compounds

Nair, Smitha,Palanisamy, P.,Sunitha, K.

, p. 663 - 667 (2022/02/22)

The oxidative cyclization of thiosemicarbazone (III) synthesized from reaction between substituted aryl aldehydes (I) with thiosemicarbazide (II) was done using ferric chloride as oxidative agent to get 2-amino-5-phenyl-1,3,4-thiadiazole (IV). 2-Amino-5-phenyl-1,3,4-thiadiazole was introduced in condensation reactions with substituted aldehydes to obtain benzylidene imine derivatives (VI)1-5. Further these were treated with sulphanilic acid to give new 2-{[5-phenyl-1,3,4-thiadiazole-2-imino] substituted benzene}diazenyl benzene sulfonic acid derivatives (VII)1-5. These derivatives were further characterized by FT-IR, 1H NMR and 13C NMR spectral studies and were screened for antibacterial, antifungal and antioxidant activities.

Synthesis and evaluation of some novel 1,3,4-thiadiazoles for antidiabetic activity

Pattan,Kittur,Sastry,Jadav,Thakur,Madamwar,Shinde

, p. 615 - 618 (2011/06/21)

A new series of 1,3,4-thiadiazole derivatives are synthesized and the structures of these compounds have been established on the basis of spectral and elemental analysis. All the compounds are evaluated for antidiabetic activity on albino rats. Most of th

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