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AA47842

13273-53-5 | 4-Bromo-1-methyl-1,2,3-triazole

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $9.00 $7.00 -   +
1g 98% in stock $13.00 $10.00 -   +
5g 98% in stock $43.00 $31.00 -   +
10g 98% in stock $85.00 $60.00 -   +
25g 98% in stock $192.00 $135.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA47842
Chemical Name: 4-Bromo-1-methyl-1,2,3-triazole
CAS Number: 13273-53-5
Molecular Formula: C3H4BrN3
Molecular Weight: 161.988
MDL Number: MFCD10696344
SMILES: Cn1nnc(c1)Br

 

Computed Properties
Complexity: 67.2  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 7  
Hydrogen Bond Acceptor Count: 2  
XLogP3: 0.7  

 

 

Upstream Synthesis Route
  • 4-Bromo-1-methyl-1H-1,2,3-triazole is a versatile building block in chemical synthesis due to its unique reactivity and structural features. This compound is commonly utilized as a substrate or intermediate in various organic reactions to introduce the 1,2,3-triazole moiety into the target molecule. One of its key applications is in the synthesis of pharmaceuticals, agrochemicals, and materials with desired properties.In organic synthesis, 4-Bromo-1-methyl-1H-1,2,3-triazole can undergo functional group transformations, such as Suzuki coupling, Sonogashira coupling, and palladium-catalyzed cross-coupling reactions, to introduce different substituents at the bromine position. This allows for the creation of diverse chemical structures for drug discovery and development.Furthermore, the 1,2,3-triazole ring in this compound serves as a versatile pharmacophore, imparting unique biological activities to the synthesized molecules. By incorporating 4-Bromo-1-methyl-1H-1,2,3-triazole into the molecular scaffold, researchers can modulate the physicochemical and pharmacokinetic properties of the final compounds, enhancing their therapeutic potential.Overall, the application of 4-Bromo-1-methyl-1H-1,2,3-triazole in chemical synthesis enables the efficient and precise construction of complex molecules with diverse functionalities, making it a valuable tool in modern organic chemistry.
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