15294-81-2 | 4,5-Dibromo-1h-1,2,3-triazole

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$8.00	$5.00
5g	97%	in stock	$13.00	$9.00
10g	97%	in stock	$15.00	$11.00
25g	97%	in stock	$36.00	$26.00
500g	97%	in stock	$637.00	$446.00

Description

• Catalog Number: AB50252
• Chemical Name: 4,5-Dibromo-1h-1,2,3-triazole
• CAS Number: 15294-81-2
• Molecular Formula: C2HBr2N3
• Molecular Weight: 226.8574
• MDL Number: MFCD08062401
• SMILES: Brc1[nH]nnc1Br
• NSC Number: 222414

Computed Properties

• Complexity: 60
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• XLogP3: 1.6

Upstream Synthesis Route

4,5-Dibromo-1H-1,2,3-Triazole, commonly known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure and reactivity make it an invaluable tool in the preparation of various organic compounds.One key application of 4,5-Dibromo-1H-1,2,3-Triazole is in the synthesis of pharmaceuticals. Its ability to serve as a building block in the construction of complex molecules makes it a valuable intermediate in drug development. By incorporating this compound into the synthesis of pharmaceutical agents, chemists can modify the properties and enhance the biological activity of potential drug candidates.Furthermore, 4,5-Dibromo-1H-1,2,3-Triazole is often utilized in the preparation of agrochemicals. Its reactivity allows for the efficient synthesis of pesticide and herbicide molecules, contributing to the development of environmentally friendly and effective agricultural products.In addition to its role in pharmaceutical and agrochemical synthesis, 4,5-Dibromo-1H-1,2,3-Triazole is also employed in material science. This compound can participate in polymerization reactions, leading to the creation of new materials with tailored properties for various applications, such as coatings, adhesives, and electronics.Overall, the versatility and reactivity of 4,5-Dibromo-1H-1,2,3-Triazole make it a valuable building block in chemical synthesis, with applications spanning the pharmaceutical, agrochemical, and materials science industries.

Literature

• Highly regioselective N-2 arylation of 4,5-dibromo-1,2,3-triazole: efficient synthesis of 2-aryltriazoles.

  Organic letters 20091105