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126158-51-8

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126158-51-8 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 15 carbon (C) atoms, 11 hydrogen (H) atoms, 1 bromine (Br) atom, and 4 nitrogen (N) atoms.

Explanation

The compound is derived from a 1H-1,2,3-triazole ring, which is a five-membered ring containing three nitrogen atoms and two carbon atoms. It has a phenyl group (a six-membered aromatic ring with alternating single and double bonds) and a bromine atom attached to the structure.

Explanation

The compound is used as a building block in the synthesis of various pharmaceuticals and biologically active molecules due to its versatile chemical structure.

Explanation

Triazoles, including this specific compound, have been found to exhibit various biological activities, such as antifungal (against fungi), antitumor (against cancer cells), and antiviral (against viruses) properties.

Explanation

Due to its biological activities and versatile chemical structure, 1H-1,2,3-Triazol-5-amine, 4-(4-bromophenyl)-1-phenylcan be a valuable compound in the development of new drugs for various medical applications.

Chemical Structure

1H-1,2,3-Triazole derivative with a substituted phenyl group and a bromine atom

Application

Organic synthesis and medicinal chemistry

Biological Activities

Antifungal, antitumor, and antiviral

Potential Use

Drug discovery and development

Check Digit Verification of cas no

The CAS Registry Mumber 126158-51-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,1,5 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 126158-51:
(8*1)+(7*2)+(6*6)+(5*1)+(4*5)+(3*8)+(2*5)+(1*1)=118
118 % 10 = 8
So 126158-51-8 is a valid CAS Registry Number.

126158-51-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-bromophenyl)-1-phenyl-1H-1,2,3-triazol-5-amine

1.2 Other means of identification

Product number -
Other names -

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:126158-51-8 SDS

126158-51-8Relevant articles and documents

Azide-acetonitrile "click" reaction triggered by Cs2CO3: The atom-economic, high-yielding synthesis of 5-amino-1,2,3-triazoles

Krishna, Patoju M.,Ramachary, Dhevalapally B.,Peesapati, Sruthi

, p. 62062 - 62066 (2015/08/03)

Medicinally important 5-amino-1,2,3-triazoles were synthesized using a novel Cs2CO3-catalyzed azide-acetonitrile[3 + 2]-cycloaddition. Aryl azides and aryl acetonitriles were employed in this transformation resulting in excellent yie

The Chemistry of 3-(α-Cyanobenzylidene)-1-phenyltriazenes and Their Conversion to Diarylmaleimides and Phenanthrene-9,10-dicarboximides

Smith, Peter A. S.,Friar, James Jeffrey,Resemann, Wolfgang,Watson, Andrew C.

, p. 3351 - 3362 (2007/10/02)

3-(α-Cyanobenzylidene)-1-phenyltriazine (3a), the product of thermolysis of 5-azido-1,4-diphenyl-1,2,3-triazole (2), is attacked by nucleophilic reagents at the azomethine carbon.Alcohols and phenol give rise to acetals of the N-phenylamidine of phenylgly

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