118946-58-0

Basic information

• Product Name: 1H-1,2,3-Triazol-5-aMine, 4-(4-chlorophenyl)-1-phenyl-
• Synonyms: 1H-1,2,3-Triazol-5-aMine, 4-(4-chlorophenyl)-1-phenyl-
• CAS NO: 118946-58-0
• Molecular Weight: 270.721
• Mol File: 118946-58-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1H-1,2,3-Triazol-5-aMine, 4-(4-chlorophenyl)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,3-Triazol-5-aMine, 4-(4-chlorophenyl)-1-phenyl-(118946-58-0)
• EPA Substance Registry System: 1H-1,2,3-Triazol-5-aMine, 4-(4-chlorophenyl)-1-phenyl-(118946-58-0)

Safety Data

• Hazardous Substances Data: 118946-58-0(Hazardous Substances Data)

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 atoms, 11 hydrogen atoms, 1 chlorine atom, and 4 nitrogen atoms.

Explanation

The compound is a derivative of 1,2,3-triazole, which is a heterocyclic compound containing a five-membered ring composed of two carbon atoms and three nitrogen atoms.

Explanation

The specific derivative has a 4-(4-chlorophenyl)-1-phenyl substituent attached to the triazole ring, which contributes to its unique properties and applications.

Explanation

The compound is useful in various medicinal and chemical applications, including organic synthesis and pharmaceutical research.

Explanation

The compound is commonly used in the development of new drugs and agrochemicals due to its unique structure and reactivity.

Explanation

The compound's structure and reactivity make it an important building block for the synthesis of diverse biologically active compounds, which can have potential applications in medicine and other fields.

Structure

1H-1,2,3-Triazole derivative

Substituent

4-(4-chlorophenyl)-1-phenyl

Applications

Medicinal and chemical applications

Usage

Development of new drugs and agrochemicals

Importance

Building block for biologically active compounds

Upstream product

• 622-37-7 Phenyl azide 
• 140-53-4 p-chlorobenzyl cyanide 

Downstream Products

• 126158-73-4 (E)-2-(4-Chloro-phenyl)-3-cyano-3,N-diphenyl-acrylamidine 
• 126158-82-5 [5-Amino-3-(4-chloro-phenyl)-4-phenyl-pyrrol-(2Z)-ylidene]-phenyl-amine 
• 118946-86-4 N-Phenyl-α,α-dimethoxy-α-(p-chlorophenyl)acetamidine 
• 126158-90-5 2-(p-Chlorophenyl)-3-phenylmaleimide 
• 118946-86-4 N-phenyl-α,α-dimethoxy-(p-chloro)phenylacetamidine 
• 118946-84-2 1-phenyl-3-(α-cyano)-(p-chloro)benzylidenetriazine 
• 118946-70-6 5-azido-4-(p-chlorophenyl)-1-phenyl-1,2,3-triazole 
• 118946-84-2 1-Phenyl-3-(α-cyano-p-chlorobenzylidene)triazene 

Relevant articles and documents

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

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