1008526-84-8 | 2-(4H-1,2,4-Triazol-4-yl)ethanamine

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$156.00	$109.00
250mg	95%	in stock	$203.00	$142.00
1g	95%	in stock	$416.00	$291.00
5g	95%	in stock	$1,490.00	$1,043.00

Description

• Catalog Number: AA03695
• Chemical Name: 2-(4H-1,2,4-Triazol-4-yl)ethanamine
• CAS Number: 1008526-84-8
• Molecular Formula: C4H8N4
• Molecular Weight: 112.1331
• MDL Number: MFCD03093052
• SMILES: NCCn1cnnc1

Upstream Synthesis Route

4-(2-Aminoethyl)-4H-1,2,4-triazole, a versatile chemical compound, serves as a valuable building block in organic synthesis. This compound finds significant application in the field of medicinal chemistry, specifically in the development of pharmaceuticals targeting diverse biological pathways. Its structural features make it a key intermediate in the synthesis of various heterocyclic compounds with potential biological activity.In chemical synthesis, 4-(2-Aminoethyl)-4H-1,2,4-triazole can be utilized as a nucleophilic reagent in the construction of complex molecules. By participating in reactions such as nucleophilic substitution, condensation, or cyclization, this compound facilitates the formation of new carbon-nitrogen bonds, essential for creating drug-like molecules with specific biological functions. Its unique triazole ring structure confers stability and reactivity, making it a valuable component in the synthesis of pharmaceutical intermediates and bioactive compounds.Furthermore, the presence of the aminoethyl functional group enables 4-(2-Aminoethyl)-4H-1,2,4-triazole to undergo various derivatization reactions, allowing for the introduction of additional substituents to tailor the compound's properties for specific applications. This flexibility in functionalization expands the compound's utility in designing novel chemical entities with potential therapeutic significance.Overall, 4-(2-Aminoethyl)-4H-1,2,4-triazole plays a crucial role in chemical synthesis by serving as a versatile and adaptable building block for the creation of structurally diverse molecules with targeted biological activities.