7343-33-1 | 5-Bromo-1h-1,2,4-triazole

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$6.00	$5.00
10g	98%	in stock	$8.00	$6.00
25g	98%	in stock	$17.00	$12.00
50g	98%	in stock	$32.00	$22.00
100g	98%	in stock	$59.00	$42.00
500g	98%	in stock	$227.00	$159.00

Description

• Catalog Number: AB48258
• Chemical Name: 5-Bromo-1h-1,2,4-triazole
• CAS Number: 7343-33-1
• Molecular Formula: C2H2BrN3
• Molecular Weight: 147.9614
• MDL Number: MFCD01421960
• SMILES: Brc1n[nH]cn1

Upstream Synthesis Route

3-Bromo-1H-1,2,4-triazole is a versatile compound widely utilized in chemical synthesis for its unique reactivity and structural properties. In organic chemistry, 3-Bromo-1H-1,2,4-triazole serves as a valuable building block for the synthesis of a variety of pharmaceuticals, agrochemicals, and fine chemicals. Its bromine substituent enhances its reactivity, making it a key intermediate in the preparation of complex molecules.One of the primary applications of 3-Bromo-1H-1,2,4-triazole is in the formation of heterocyclic compounds, where its triazole ring confers specific properties and functionalities to the final products. By incorporating 3-Bromo-1H-1,2,4-triazole into synthetic pathways, chemists can introduce a diverse range of chemical functionalities, enabling the modification of biological activities or physical properties of the target molecules.Furthermore, 3-Bromo-1H-1,2,4-triazole can participate in various key reactions such as nucleophilic substitution, Suzuki coupling, and transition metal-catalyzed cross-coupling reactions. These reactions enable the selective modification of the triazole ring, leading to the creation of structurally diverse compounds with tailored properties. Additionally, the bromine atom in 3-Bromo-1H-1,2,4-triazole can serve as a handle for further derivatization, allowing for the introduction of additional functional groups or labels.Overall, the strategic incorporation of 3-Bromo-1H-1,2,4-triazole in chemical synthesis offers chemists a powerful tool for the construction of molecular scaffolds with diverse applications in medicinal chemistry, materials science, and agrochemical research. Its versatility and reactivity make it an indispensable building block for the creation of novel compounds with enhanced functionalities and potential biological activities.