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1,2,4-Triazolo[3,4-b][1,3,4]thiadiazol-6-amine, N,3-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113486-75-2

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113486-75-2 Usage

Explanation

This is the full chemical name of the compound, which is a derivative of the thiadiazole family.

Explanation

The compound belongs to the thiadiazole family, which is a group of chemical compounds with a specific ring structure.

Explanation

The compound has potential uses in the fields of biology and pharmaceuticals due to its unique chemical properties.

Explanation

Research has been conducted to explore the compound's effectiveness in fighting cancer cells.

Explanation

Studies have shown that the compound may have the ability to reduce inflammation, which could be useful in treating various inflammatory conditions.

Explanation

The compound has been researched for its potential to inhibit the growth of microorganisms, which could be beneficial in the development of new antimicrobial drugs.

Explanation

The compound's unique properties make it a candidate for the development of new drugs to treat a range of medical conditions.

Explanation

Due to its various properties, the compound has a wide range of potential applications in the medical and pharmaceutical industries.

Family

Thiadiazole

Potential Applications

Biological and Pharmaceutical

Anti-cancer Properties

Studied for potential use as an anti-cancer agent

Anti-inflammatory Properties

Indicated by research

Antimicrobial Properties

Investigated for potential use

Drug Development

Investigated for new drugs for various medical conditions

Diverse Potential Uses

Field of medicine and pharmaceuticals

Check Digit Verification of cas no

The CAS Registry Mumber 113486-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,4,8 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113486-75:
(8*1)+(7*1)+(6*3)+(5*4)+(4*8)+(3*6)+(2*7)+(1*5)=122
122 % 10 = 2
So 113486-75-2 is a valid CAS Registry Number.

113486-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,3-diphenyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-amine

1.2 Other means of identification

Product number -
Other names 3-Phenyl-6-phenylamino-s-triazolo<3,4-b><1,3,4>thiadiazole

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:113486-75-2 SDS

113486-75-2Downstream Products

113486-75-2Relevant academic research and scientific papers

A Convenient and Novel Synthesis of 1,2,4-Triazolo-thiadiazoles as Potential Pesticides

Chaturvedi, Bandana,Tiwari, Nirupama,Nizamuddin

, p. 1229 - 1232 (2007/10/02)

6-Arylamino-1,2,4-triazolo-thiadiazoles (IV) were synthesized by cyclo-dehydro-sulphurization of corresponding thioureas (III), which in turn were prepared by the condensation of N-amino-3-mercapto-1,2,4-triazoles (II) and aryl isothiocyanates (I) in dry dimethylformamide.These triazolo thiadiazoles (IV) were screened for their fungicidal activities of A. niger and H. oryzae.

Synthesis of Heterocycles. Part VII . Synthesis and Antimicrobial Activity of Some 7H-s-Triazolothiadiazine and s-Triazolothiadiazole Derivatives

Eweiss, N. F.,Bahajaj, A. A.

, p. 1173 - 1182 (2007/10/02)

The cyclization of 4-amino-5-aryl-3-cyanomethylthio-1,2,4-triazoles II in the presence of concentrated sulfuric acid yields 7H-6-amino-s-triazolothiadiazines III.Cyclization of 4-amino-5-aryl-1,2,4-triazole-3-thiones I with phenacyl chloride yields 7H-3-aryl-6-phenyl-s-triazolothiadiazines IV.Similarly, compounds I condensed with cyanogen bromide, phenyl isothiocyanate and carbon disulfide to give the corresponding cyclized products 6-amino-3-aryl-s-triazolothiadiazoles V, 3-aryl-6-phenylamino-s-triazolothiadiazoles VI and 3-aryl-s-triazolothiadiazol-6(5H)thiones VII, respectively.Also in the presence of phosphoryl chloride, compounds I underwent cyclization with monocarboxylic acids and oxalic acid to 3,6-diaryl-s-triazolothiadiazole VIII and 6,6'-bis(3-aryl-s-triazolothiadiazoles) IX.The above compounds were screened for their antimicrobial activity.

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